Variant DetailsVariant: dgv5477n54Internal ID | 20138901 | Landmark | | Location Information | | Cytoband | 17p11.2 | Allele length | Assembly | Allele length | hg38 | 63896 | hg19 | 63896 | hg18 | 63896 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv574497, nsv574495, nsv574501, nsv574496, nsv574503, nsv574499, nsv574498, nsv574500, nsv574502 | Samples | | Known Genes | CCDC144A, FAM106CP, USP32P1 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | dgv5477n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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