CNAs and UPDs identified at diagnosis and relapse by SNP profiling
| Aberration . | Candidate genes in CDR . | Diagnosis . | Lost . | Acquired . | Relapse . |
|---|---|---|---|---|---|
| del(9q21) | HNPRK, NTRK2 | 6 | –3 | 3 | |
| UPD13q | FLT3 | 4 | –1 | +7 | 10 |
| UPD1p | ? | 1 | –1 | 0 | |
| Nonrecurrent CNAs at diagnosis | 4 | –2 | 2 | ||
| gain(11q23.3) | MLL | 0 | +3 | 3 | |
| del(12p13) | ETV6 | 0 | +3 | 3 | |
| del(11p13) | WT1 | 0 | +3 | 3 | |
| del(17p) | TP53 | 0 | +2 | 2 | |
| del(17q11.2) | NF1 | 0 | +2 | 2 | |
| del(3p14.2) | FHIT | 0 | +2 | 2 | |
| del(4q22.1) | ? | 0 | +2 | 2 | |
| Trisomy 5 | ? | 0 | +1 | 1 | |
| Monosomy 7 | ? | 0 | +1 | 1 | |
| Nonrecurrent CNAs at relapse | 0 | +22 | 22 | ||
| Total | 15 | –7 | +48 | 56 |
| Aberration . | Candidate genes in CDR . | Diagnosis . | Lost . | Acquired . | Relapse . |
|---|---|---|---|---|---|
| del(9q21) | HNPRK, NTRK2 | 6 | –3 | 3 | |
| UPD13q | FLT3 | 4 | –1 | +7 | 10 |
| UPD1p | ? | 1 | –1 | 0 | |
| Nonrecurrent CNAs at diagnosis | 4 | –2 | 2 | ||
| gain(11q23.3) | MLL | 0 | +3 | 3 | |
| del(12p13) | ETV6 | 0 | +3 | 3 | |
| del(11p13) | WT1 | 0 | +3 | 3 | |
| del(17p) | TP53 | 0 | +2 | 2 | |
| del(17q11.2) | NF1 | 0 | +2 | 2 | |
| del(3p14.2) | FHIT | 0 | +2 | 2 | |
| del(4q22.1) | ? | 0 | +2 | 2 | |
| Trisomy 5 | ? | 0 | +1 | 1 | |
| Monosomy 7 | ? | 0 | +1 | 1 | |
| Nonrecurrent CNAs at relapse | 0 | +22 | 22 | ||
| Total | 15 | –7 | +48 | 56 |
For the complete list, see supplementary Tables 1 to 3. CDR, commonly deleted region.