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Searched: Craniosynostosis and Related Disorders Sequencing Panel with CNV Detection
Search Results
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…variants (CNVs). This panel will detect all these variant types. Notably, the vast majority of CNVs, including 16p11.2 deletion syndrome and Smith-Magenis syndrome (17p11.2) will be detected. This panel is not designed to diagnose Prader…
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Test CodeMethodPrice10197Sequencing with CNV PGxome$990
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Test CodeMethodPrice8237Sequencing with CNV PGxome$9902956Sanger Sequencing$870
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Test CodeMethodPrice959Sanger Sequencing$4909087Sequencing with CNV PGxome$990
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Test CodeMethodPrice11735Sequencing with CNV PGxome$9902514Sanger Sequencing$1280
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Test CodeMethodPrice4929Sequencing with CNV PGxome$990
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Test CodeMethodPrice13041Sequencing with CNV PGxome$1190
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Test CodeMethodPrice3003Sequencing with CNV PGxome$990
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Test CodeMethodPrice3005Sequencing with CNV PGxome$990
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Test CodeMethodPrice179Sanger Sequencing$8408297Sequencing with CNV PGxome$990
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Test CodeMethodPrice174Sanger Sequencing$6108751Sequencing with CNV PGxome$990
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Test CodeMethodPrice178Sanger Sequencing$6508657Sequencing with CNV PGxome$990
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Test CodeMethodPrice10343Sequencing with CNV PGxome$990
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Test CodeMethodPrice11331Sequencing with CNV PGxome$990499Sanger Sequencing$1100
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Test CodeMethodPrice2103Sanger Sequencing$4409213Sequencing with CNV PGxome$990
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Test CodeMethodPrice4361Sequencing with CNV PG-Select$990
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Test CodeMethodPrice2057MLPA$540
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Test CodeMethodPrice2871Sanger Sequencing$5803469Sequencing with CNV PGxome$990
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Test CodeMethodPrice429Sanger Sequencing$9709245Sequencing with CNV PGxome$990
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Test CodeMethodPrice428Sanger Sequencing$560
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