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.
- One 20‑μL gDNA (10 ng/μL) specimen
- Shipment A: June 14
- Shipment B: December 13