Variant DetailsVariant: nsv545838Internal ID | 15986561 | Landmark | | Location Information | | Cytoband | 1p36.11 | Allele length | Assembly | Allele length | hg38 | 61412 | hg19 | 61412 | hg18 | 61412 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv201n54 | Supporting Variants | nssv711737, nssv711731, nssv711735, nssv711740, nssv711736, nssv711738, nssv711739, nssv711733, nssv711734, nssv711732, nssv711730 | 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) | nsv545838
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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