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. 2017 Aug 14;13(8):e1006959. doi: 10.1371/journal.pgen.1006959

Table 1. Mutations present in tumour samples.

Comparison # SNVs # indels
sibling_tissue_1.vs.control_tissue_1 944 7221
control_tissue_1.vs.tumour_tissue_1 485 1
sibling_tissue_2.vs.control_tissue_2a 995 6959
sibling_tissue_2.vs.control_tissue_2b 1001 9747
control_tissue_2a.vs.tumour_tissue_2a 592 1
control_tissue_2b.vs.tumour_tissue_2b 526 1
sibling_tissue_3.vs.control_tissue_3 866 7829
control_tissue_3.vs.tumour_tissue_3 465 1

Whole exome sequencing was performed on dissected tumours, adjacent non-tumour control tissue and siblings. The number of SNVs and indels detected in sibling vs control tissue and control vs tumour tissue are shown.