Variant DetailsVariant: nsv545863Internal ID | 15986586 | Landmark | | Location Information | | Cytoband | 1p36.11 | Allele length | Assembly | Allele length | hg38 | 12729 | hg19 | 12729 | hg18 | 12729 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv711803, nssv711809, nssv711813, nssv711810, nssv711804, nssv711811, nssv711814, nssv711818, nssv711819, nssv711815, nssv711805, nssv711807, nssv711816, nssv711812, nssv711806, nssv711808, nssv711817 | Samples | | Known Genes | RHD | 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) | nsv545863
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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