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Searched: Hypertrophic Cardiomyopathy Sequencing Panel with CNV Detection
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Test CodeMethodPrice1313Sequencing with CNV PGxome$990
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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 CodeMethodPrice198Sanger Sequencing$10604545Sequencing with CNV PGxome$990
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Test CodeMethodPrice196Sanger Sequencing$5408997Sequencing with CNV PGxome$990
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Test CodeMethodPrice11487Sequencing with CNV PGxome$990197Sanger Sequencing$1560
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Test CodeMethodPrice11793Sequencing with CNV PGxome$990144Sanger Sequencing$1130
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Test CodeMethodPrice148Sanger Sequencing$3709233Sequencing with CNV PGxome$990
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Test CodeMethodPrice177Sanger Sequencing$6808557Sequencing with CNV PGxome$990
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Test CodeMethodPrice173Sanger Sequencing$13803131Sequencing with CNV PGxome$990
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Test CodeMethodPrice175Sanger Sequencing$5808881Sequencing with CNV PGxome$990
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Test CodeMethodPrice194Sanger Sequencing$5409003Sequencing with CNV PGxome$990
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Test CodeMethodPrice176Sanger Sequencing$5408999Sequencing 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 CodeMethodPrice11489Sequencing with CNV PGxome$990172Sanger Sequencing$1590
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Test CodeMethodPrice5263Sequencing with CNV PGxome$1290
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Test CodeMethodPrice1339Sequencing with CNV PGxome$990
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Test CodeMethodPrice1250Sanger Sequencing$5808831Sequencing with CNV PGxome$990
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Test CodeMethodPrice2609Sequencing with CNV PGxome$990
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