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. 2017 Jun 27;8(37):61538–61550. doi: 10.18632/oncotarget.18618

Figure 1. Somatic SNVs and CNVs in genomes of 70 Korean patients with TNBC.

Figure 1

(A) Percentages of types of somatic mutations, showing that a high percentage consisted of novel somatic SNVs. (B) Numbers of somatic SNVs and CNVs in individual patients. The numbers of genes with homozygous deletions per patient ranged from 1 to 170, whereas the numbers of amplified genes per patient ranged from 0 to 214. SNVs, single nucleotide variants; CNVs, copy number variations; TNBC, triple-negative breast cancer.