Table 2 Published reports: summary of intrachromosomal copy number changes detected by array CGH.
Paper | No of patients* | Intrachromosomal | No of targets on array | ||
---|---|---|---|---|---|
De novo | Familial | Unknown | |||
Vissers L et al10 | 20 (0) | 2 | 2 | 1 | 3569 |
Shaw‐Smith et al11 | 50 (41) | 7 | 5 | 0 | ∼3500 |
Rosenberg et al13 | 81(0) | 4 | 7 | 3 | ∼3500 |
Schoumans et al14 | 41(41) | 4 | 0 | 0 | 2600 |
This study | 140 (31) | 11 | 7 | 3 | ∼3500 |
Total | 332 | 28 | 21 | 7 | |
De Vries et al12 | 100 | 10 | 0 | 5 | 32447 |
*Number on which subtelomeric imbalances have been excluded before array CGH was carried out.
CGH, comparative genomic hybridisation.