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Neuroblastoma Panel

Summary and Pricing

Test Method

Exome Sequencing with CNV Detection
Test Code Test Copy Genes Gene CPT Codes Copy CPT Codes
ALK 81479,81479
KIF1B 81479,81479
PHOX2B 81404,81403
Test Code Test Copy Genes Panel CPT Code Gene CPT Codes Copy CPT Code Base Price
5057Genes x (3)81479 81403(x1), 81404(x1), 81479(x4) $990 Order Options and Pricing

Pricing Comments

We are happy to accommodate requests for testing single genes in this panel or a subset of these genes. The price will remain the list price. If desired, free reflex testing to remaining genes on panel is available. Alternatively, a single gene or subset of genes can also be ordered via our Custom Panel tool.

An additional 25% charge will be applied to STAT orders. STAT orders are prioritized throughout the testing process.

Click here for costs to reflex to whole PGxome (if original test is on PGxome Sequencing platform).

Click here for costs to reflex to whole PGnome (if original test is on PGnome Sequencing platform).

Turnaround Time

3 weeks on average for standard orders or 2 weeks on average for STAT orders.

Please note: Once the testing process begins, an Estimated Report Date (ERD) range will be displayed in the portal. This is the most accurate prediction of when your report will be complete and may differ from the average TAT published on our website. About 85% of our tests will be reported within or before the ERD range. We will notify you of significant delays or holds which will impact the ERD. Learn more about turnaround times here.

Targeted Testing

For ordering sequencing of targeted known variants, go to our Targeted Variants page.


Genetic Counselors


  • Yuan Xue, PhD

Clinical Features and Genetics

Clinical Features

Neuroblastoma is the most common type of childhood cancer that occurs before 1 year of age, accounting for 10-15% of cancer deaths in children. Approximately 90% of neuroblastomas are detected by 5 years of age, while 30% are found in the first year of life with the median age of diagnosis of 22 months (Esiashvili Natia et al. 2009). This tumor type can occur in adolescence and adulthood, although the prognosis is poorer compared to a childhood incidence (Colon and Chung 2011). The majority of neuroblastomas (65%) arise in the abdomen, with half of these in the medulla of the adrenal gland. They can also occur in the chest (20%), neck (5%), pelvis (5%), and in 1% of cases have an unknown primary (Colon and Chung 2011). Symptoms of patients with neuroblastoma include malaise, fevers, weight loss, enlarging mass, pain, and abdominal distention. Other symptoms can include early-onset hypertension and tachycardia due to the secretion of catecholamines. Neuroblastomas commonly occur sporadically in a family, but 1-2% of cases occur with family histories of neuroblastoma. Hereditary neuroblastomas tend to have earlier presentations and lead to multiple primary cancers. They also show significant clinical heterogeneity, whereby a pedigree may show an individual with spontaneous cancer regression, whereas another individual with metastatic spread (Deyell and Attiyeh 2011). Siblings of an affected patient with neuroblastoma have a 10-fold increase in developing neuroblastoma (Friedman 2005). Neuroblastomas can also be found with other conditions such as Hirschsprung disease, congenital hypoventilation disorder, and neurofibromatosis type 1 (Greengard and Park 2012).


Hereditary neuroblastoma is an autosomal dominant disorder that shows incomplete penetrance (Fisher and Tweddle 2012). Neuroblastomas show whole-chromosome gains and segmental chromosomal aberrations. The former results from hyperdiploidy and has a favorable prognosis, whereas the latter is associated with MYCN amplification and associated with worse outcomes (Colon and Chung 2011). The most frequent genetic aberration is an unbalanced chromosome 17q gain found in 70% of neuroblastomas, which has a poor prognosis (Bown et al. 1999).

In cases of hereditary neuroblastoma, the most common etiology are pathogenic variants in the anaplastic lymphoma kinase (ALK) oncogene. ALK encodes a tyrosine kinase receptor involved in cellular differentiation, proliferation, and survival. Pathogenic variants lead to constitutive activation of kinase activity. ALK pathogenic variants are rarely found in simplex cases (Mosse et al. 2008). All reported ALK causative variants have been missense, with the majority in the kinase domain (Human Gene Mutation Database).

Another cause of hereditary neuroblastomas are PHOX2B pathogenic variants, which are often associated with Hirschsprung's disease and/or congenital hypoventilation (Mosse et al. 2004). PHOX2B encodes a transcription factor that is involved in the normal sympathetic neuronal development and catecholamine synthesis. PHOX2B pathogenic variants are rarely found in sporadic neuroblastomas (van Limpt et al. 2004). The majority of causative PHOX2B variants include missense and small insertions and deletions (Human Gene Mutation Database).

Germline pathogenic variants in KIF1B in individuals with neuroblastoma and pheochromocytomas, and possibly nonneural tumors, have been reported (Schlisio et al. 2008; Yeh IT et al. 2008). The majority of KIF1B causative variants are missense changes (Human Gene Mutation Database).

Clinical Sensitivity - Sequencing with CNV PGxome

Taken together, ALK and PHOX2B germline pathogenic variants account for 90% of hereditary neuroblastoma, with the majority being in the ALK gene (Fisher and Tweddle 2012).

Clinical sensitivity for KIF1B pathogenic variants is unknown at this time since relatively few individuals with these variants have been reported.

No gross deletions or duplications have been reported for these genes for neuroblastoma. They are expected to be rare.

Testing Strategy

This test is performed using Next-Gen sequencing with additional Sanger sequencing as necessary.

This panel provides 100% coverage of all coding exons of the genes plus 10 bases of flanking noncoding DNA in all available transcripts along with other non-coding regions in which pathogenic variants have been identified at PreventionGenetics or reported elsewhere. We define full coverage as >20X NGS reads or Sanger sequencing. PGnome panels typically provide slightly increased coverage over the PGxome equivalent. PGnome sequencing panels have the added benefit of additional analysis and reporting of deep intronic regions (where applicable).

Sanger sequencing of PHOX2B exon 3 for detection of the polyalanine repeat region is not performed as part of this test.

Dependent on the sequencing backbone selected for this testing, discounted reflex testing to any other similar backbone-based test is available (i.e., PGxome panel to whole PGxome; PGnome panel to whole PGnome).

Indications for Test

Hereditary neuroblastoma should be suspected in neonates where there is a family history of neuroblastoma, ganglioneuroma, or ganglioneuroblastoma in two or more 1st degree relatives or in bilateral neuroblastoma (Bourdeaut et al. 2012). Genetic testing for ALK pathogenic variants should also be carried out to detect subclinical disease and to indicate the likelihood of developing neuroblastoma. Germline pathogenic variants in this gene should also be tested in minors with a family history of neuroblastoma. Prenatal diagnosis for pregnancies at increased risk for ALK-related neuroblastoma susceptibility is possible; however, such testing cannot predict if neuroblastoma will develop (Greengard and Park. 2012).


Official Gene Symbol OMIM ID
ALK 105590
KIF1B 605995
PHOX2B 603851
Inheritance Abbreviation
Autosomal Dominant AD
Autosomal Recessive AR
X-Linked XL
Mitochondrial MT


Name Inheritance OMIM ID
Neuroblastoma 1 AD 256700
Neuroblastoma 2 AD 613013
Neuroblastoma 3 AD 613014

Related Test



  • Bourdeaut F. et al. 2012. European Journal of Human Genetics. 20: 291-7. PubMed ID: 22071890
  • Bown N. et al. 1999. The New England Journal of Medicine. 340: 1954-61. PubMed ID: 10379019
  • Colon N.C., Chung D.H. 2011. Advances in Pediatrics. 58: 297-311. PubMed ID: 21736987
  • Deyell R.J., Attiyeh E.F. 2011. Cancer Genetics. 204: 113-21. PubMed ID: 21504710
  • Esiashvili N. et al. 2009. Current Problems in Cancer. 33: 333-60. PubMed ID: 20172369
  • Fisher J.P, Tweddle D.A. 2012. Seminars in Fetal & Neonatal Medicine. 17: 207-15. PubMed ID: 22673527
  • Friedman D. L. 2005. Cancer Epidemiology Biomarkers & Prevention. 14: 1922-7. PubMed ID: 16103438
  • Greengard and Park. 2012. ALK-Related Neuroblastic Tumor Susceptibility. In: Pagon RA, Adam MP, Bird TD, Dolan CR, Fong C-T, Smith RJ, and Stephens K, editors. GeneReviews™, Seattle (WA): University of Washington, Seattle. PubMed ID: 20301782
  • Human Gene Mutation Database (Bio-base).
  • Mosse Y.P. et al. 2004. American Journal of Human Genetics. 75: 727-30. PubMed ID: 15338462
  • Mossé Y.P. et al. 2008. Nature. 455: 930-5. PubMed ID: 18724359
  • Schlisio S. et al. 2008. Genes & Development. 22: 884-93. PubMed ID: 18334619
  • van Limpt V. et al. 2004. Oncogene. 23: 9280-8. PubMed ID: 15516980
  • Yeh I.T. et al. 2008. Human Genetics. 124: 279-85. PubMed ID: 18726616


Ordering Options

We offer several options when ordering sequencing tests. For more information on these options, see our Ordering Instructions page. To view available options, click on the Order Options button within the test description.

myPrevent - Online Ordering

  • The test can be added to your online orders in the Summary and Pricing section.
  • Once the test has been added log in to myPrevent to fill out an online requisition form.
  • PGnome sequencing panels can be ordered via the myPrevent portal only at this time.

Requisition Form

  • A completed requisition form must accompany all specimens.
  • Billing information along with specimen and shipping instructions are within the requisition form.
  • All testing must be ordered by a qualified healthcare provider.

For Requisition Forms, visit our Forms page

If ordering a Duo or Trio test, the proband and all comparator samples are required to initiate testing. If we do not receive all required samples for the test ordered within 21 days, we will convert the order to the most effective testing strategy with the samples available. Prior authorization and/or billing in place may be impacted by a change in test code.

Specimen Types

Specimen Requirements and Shipping Details

PGxome (Exome) Sequencing Panel

PGnome (Genome) Sequencing Panel

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Note: acceptable specimen types are whole blood and DNA from whole blood only.
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