Variant DetailsVariant: nsv586129Internal ID | 16026852 | Landmark | | Location Information | | Cytoband | 20q13.12 | Allele length | Assembly | Allele length | hg38 | 23358 | hg19 | 23358 | hg18 | 23351 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv7592n54 | Supporting Variants | nssv1150952, nssv1150954, nssv1150951, nssv1150949, nssv1150953, nssv1150950 | Samples | HGDP00795, HGDP00797, HGDP00806, HGDP00799, HGDP01079, HGDP01376 | Known Genes | | 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) | nsv586129
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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