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Table 1 Allelic counts for tumor sample SU070 from Jan et al.[17]

From: Inferring clonal evolution of tumors from single nucleotide somatic mutations

SNV Variant allele read counts Read depth Allele frequency Cluster ID
CACNA1H 12,085 24,860 0.486 (95% CI: 0.481-0.491) A
TET2-T1884A 4,220 8,772 0.481 (95% CI: 0.472-0.490) B
TET2-Y1649stop 7,792 16,211 0.481 (95% CI: 0.474-0.487) A
CXorf66 3,684 8,150 0.452 (95% CI: 0.443-0.461) B
CXorf36 3,523 8,060 0.437 (95% CI: 0.428-0.446) A
DOCK9 3,391 8,676 0.391 (95% CI: 0.382-0.400) C
NCRNA00200 9,201 25,413 0.362 (95% CI: 0.357-0.367) C
CTCF 10,558 30,119 0.351 (95% CI: 0.346-0.355) C
GABARAPL1 1,648 4,992 0.330 (95% CI: 0.319-0341) C
SCN4B 5,113 16,386 0.312 (95% CI: 0.306-0.318) C