Table 3.
Regions identified that contain genes with known alterations in human cancer
| Region | Genes |
|---|---|
| Amplifications | |
| 1q21-q44 | ABL2, FCGR2B, FH, HRPT2, IRTA1, PBX1, SDHC, TPR |
| 2p24 | MYCN |
| 2p24-p16 | ALK, BCL11A, MSH2, MSH6 |
| 3q27-q27 | EIF4A2 |
| 7p21-p11 | HOXA13, JAZF1, ZNFN1A1 |
| 7q31-q35 | BRAF, TIF1 |
| 8q11-q22 | NBS1, NCOA2, PLAG1 |
| 8q24-q24 | EXT1 |
| 12p13-p12 | HIST1H4I, CCND2, ETV6, KRAS |
| 12q14-q15 | HMGA2 |
| 13q14 | FOXO1A |
| 14q11 | TCR-α |
| 17q21-q25 | BRIP1, CLTC, COL1A1, HLF, MSI2, PRKAR1A |
| 20q11-q13 | GNAS |
| Deletions | |
| 1p36-p36 | PAX7, PRDM16 |
| 9p21 | CDKN2A/2B |
| 14q11 | TCR-α |