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Please log in to determine if you are eligible to purchase PT Programs.
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COPY NUMBER VARIANT SOLID TUMOR - CNVST |
CNVST
Analytes/procedures in bold type are regulated for proficiency testing by the Centers for Medicare & Medicaid Services (CMS).
Additional Information/Minimum Requirements
- This program is designed for laboratories using next-generation sequencing for copy number analysis.
- Laboratories will be asked to identify copy number alterations in some of these genes: CDKN2A, CDKN2B, EGFR, ERBB2, FGFR3, MET, MYC, MYCN, TP53.
- Copy number alterations tested will include amplification, gain, copy neutral loss of heterozygosity, and deletion.
Program Information
- One 20‐µL gDNA (10ng/µL) specimen
Shipping Schedule
- Shipment A: June 13
- Shipment B: December 12
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