| Â | 1M | 660W | Omni1 | CytoSNP12 |
|---|
Accession
| GSE16894 | GSE17208 | GSE17197 | GSE17123 |
# Trios
| 27 | 27 | 27 | 27 |
Markers
| 1128030 | 634750 | 1014080 | 277297 |
CNV-specific
| 29367 | 62095 | 88450 | 467 |
Date Processed
| 5/19/2008 | 2/10/2009 | 6/29/2009 | 7/1/2009 |
Abnormalities:
| Â | Â | Â | Â |
AMP
| 77 | 63 | 84 | 18 |
DEL
| 225 | 248 | 277 | 8 |
HD
| 401 | 3877 | 4231 | 17 |
UPhD
| 0 | 0 | 0 | 0 |
UPiD
| 9 | 13 | 10 | 6 |
Unk
| 159 | 50 | 108 | 20 |
Total
|
871
|
4251
|
4710
|
69
|
- 1M: Human1M-Duov3; 660W: Human660W-Quadv1; Omni1: HumanOmni1-Quadv1; CytoSNP12: HumanCytoSNP-12v2-1; Accession: accession identifier in the NCBI GEO database; Markers: approximate number of autosomal markers following conversion; CNV-specific: the number of autosomal CNV-specific probes; Date Processed: the processing date reported in the Illumina final report. AMP amplification, DEL hemizygous deletion, HD homozygous deletion, UPhD uniparental heterodisomy, UPiD uniparental isodisomy, Unk detected abnormalities of undetermined type.
