Figure 2. Patients With a Pathogenic/Likely Pathogenic (P/LP) Germline Variant and Any Pathogenic (P) Somatic Variant and/or Copy Number Loss (CNL) in the Same Gene Across All Cancer Types.

As the y-axis is the number of patients with any germline finding, the top of the bar represents the total number of patients with a germline finding in the respective gene. Light and dark blue bars are mutually exclusive.