Variant DetailsVariant: esv3623061Internal ID | 6663229 | Landmark | | Location Information | | Cytoband | 10q11.21 | Allele length | Assembly | Allele length | hg38 | 2042 | hg19 | 2042 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13764992, essv13764993, essv13764991, essv13764996, essv13764998, essv13764995, essv13764997, essv13764994, essv13764990, essv13764999 | Samples | HG01173, NA07347, HG00311, HG01628, HG00323, NA20800, HG02554, NA06989, HG00280, HG00343 | Known Genes | | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3623061
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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