Chr. | Start–end band | Genomic position: start–end GRCh37/hg19 | Variant type | Size (Mb) | COSMIC census cancer gene(s) within the region |
---|---|---|---|---|---|
7 | p22.3p22.1 | 45,130–4,642,192 | 1 copy gain | 4.6 | CARD11 |
7 | q21.3q36.3 | 96,556,335–159,128,556 | 1 copy gain | 62.6 | TRRAP, CUX1, CREB3L2, MET, POT1, SND1, SMO, TRB, TRIM24, KIAA1549, BRAF, FAM131B, CNTNAP2, EZH2, KMT2C, MNX1 |
11 | q24.2q25 | 125,246,792–134,945,165 | 1 copy loss | 9.7 | FLI1, KCNJ5 |
18 | p11.22p11.21 | 9,095,620–14,089,409 | 1 copy gain | 4.99 | |
18 | q11.1q23 | 18.550.472–78.012.829 | 1 copy gain | 59.5 | ZNF521,SS18, SETBP1, SMAD2, SMAD4, DCC, MALT1, BCL2, KDSR, |