Variant DetailsVariant: esv3585522Internal ID | 6625840 | Landmark | | Location Information | | Cytoband | 1p36.11 | Allele length | Assembly | Allele length | hg38 | 68581 | hg19 | 68581 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv9893102, essv9893105, essv9893101, essv9893100, essv9893104, essv9893109, essv9893103, essv9893107, essv9893108, essv9893106, essv9893110 | Samples | HG02944, HG01462, HG00102, NA19204, HG02078, NA19026, HG03756, HG02979, NA18646, HG03025, NA12776 | Known Genes | RHD | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3585522
| Frequency | Sample Size | 2504 | Observed Gain | 11 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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