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Searched: Congenital Muscular Dystrophy Sequencing Panel with CNV Detection
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Test CodeMethodPrice10379Sequencing 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 CodeMethodPrice10339Sequencing with CNV PGxome$990
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Test CodeMethodPrice11171Sequencing with CNV PGxome$990912Sanger Sequencing$710
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Test CodeMethodPrice11441Sequencing with CNV PGxome$990345Sanger Sequencing$2580
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Test CodeMethodPrice354Sanger Sequencing$350
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Test CodeMethodPrice10401Sequencing with CNV PGxome$990
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Test CodeMethodPrice245Sanger Sequencing$350
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Test CodeMethodPrice11701Sequencing with CNV PGxome$990874Sanger Sequencing$2170
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Test CodeMethodPrice7633Sequencing with CNV PG-Select$990
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Test CodeMethodPrice10433Sequencing with CNV PGxome$1290
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Test CodeMethodPrice2973Sanger Sequencing$7508429Sequencing with CNV PGxome$990
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Test CodeMethodPrice11759Sequencing with CNV PGxome$9901739Sanger Sequencing$1190
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Test CodeMethodPrice2153Sanger Sequencing$9103833Sequencing with CNV PGxome$990
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Test CodeMethodPrice7649Sequencing with CNV PG-Select$990
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Test CodeMethodPrice4567Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7029Sequencing with CNV PG-Select$990
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Test CodeMethodPrice1492Sanger Sequencing$61010009Sequencing with CNV PGxome$990
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Test CodeMethodPrice10183Sequencing with CNV PGxome$990
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Test CodeMethodPrice1418Sanger Sequencing$5408981Sequencing with CNV PGxome$990
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