SALSA^® digitalMLPA™ D001 Hereditary Cancer Panel 1 can detect copy number variation (CNV) in 28 clinically relevant oncogenes. CNVs in these genes are associated with hereditary predisposition to one or more of the following cancer types: breast, ovarian, colorectal, gastric, prostate, pancreatic, endometrial, and melanoma.

Learn more about our digitalMLPA technique in this brochure or on this page.