Extended Data Fig. 4: Somatic mutation frequencies in genes recurrently mutated in breast cancer.

Visualisation of SNVs and CNAs across all interrogated genes in patients co-consented to a parallel tumor sequencing study (PBCP, n = 53 patients).

Visualisation of SNVs and CNAs across all interrogated genes in patients co-consented to a parallel tumor sequencing study (PBCP, n = 53 patients).