Frequency of aCGH copy number aberrations associated with poor prognosis
| Aberration . | Frequency AA patients, % (n) . | Frequency EA patients, % (n) . | P value (Fisher’s) . | Corrected P value . | Refs . |
|---|---|---|---|---|---|
| 1p deletion | 58 (26/45) | 51 (99/196) | .412 | .774 | 24,25 |
| p18 deletion | 40 (18/45) | 28 (54/196) | .107 | .374 | 25,26 |
| p18 homozygous deletion | 4 (2/45) | 3 (6/196) | .645 | .774 | 25 |
| 1q gain | 33 (15/45) | 56 (110/196) | .008 | .094 | 24,25 |
| 8p deletion | 49 (22/45) | 45 (89/196) | .741 | .808 | 27 |
| 13q deletion | 40 (18/45) | 46 (90/196) | .510 | .774 | 21,24,28 |
| 13 monosomy | 29 (13/45) | 34 (66/196) | .600 | .774 | 21,24 |
| 14q deletion | 29 (13/45) | 43 (85/196) | .092 | .374 | 29 |
| 16q deletion | 33 (15/45) | 39 (76/196) | .609 | .774 | 29,30 |
| 17p deletion | 4 (2/45) | 13 (25/196) | .125 | .374 | 27 |
| 22q deletion | 20 (9/45) | 26 (51/196) | .450 | .774 | 29 |
| Aberration . | Frequency AA patients, % (n) . | Frequency EA patients, % (n) . | P value (Fisher’s) . | Corrected P value . | Refs . |
|---|---|---|---|---|---|
| 1p deletion | 58 (26/45) | 51 (99/196) | .412 | .774 | 24,25 |
| p18 deletion | 40 (18/45) | 28 (54/196) | .107 | .374 | 25,26 |
| p18 homozygous deletion | 4 (2/45) | 3 (6/196) | .645 | .774 | 25 |
| 1q gain | 33 (15/45) | 56 (110/196) | .008 | .094 | 24,25 |
| 8p deletion | 49 (22/45) | 45 (89/196) | .741 | .808 | 27 |
| 13q deletion | 40 (18/45) | 46 (90/196) | .510 | .774 | 21,24,28 |
| 13 monosomy | 29 (13/45) | 34 (66/196) | .600 | .774 | 21,24 |
| 14q deletion | 29 (13/45) | 43 (85/196) | .092 | .374 | 29 |
| 16q deletion | 33 (15/45) | 39 (76/196) | .609 | .774 | 29,30 |
| 17p deletion | 4 (2/45) | 13 (25/196) | .125 | .374 | 27 |
| 22q deletion | 20 (9/45) | 26 (51/196) | .450 | .774 | 29 |