Variant DetailsVariant: esv3610429Internal ID | 6650655 | Landmark | | Location Information | | Cytoband | 6q22.1 | Allele length | Assembly | Allele length | hg38 | 7888 | hg19 | 7888 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12508960, essv12508957, essv12508953, essv12508961, essv12508954, essv12508963, essv12508958, essv12508955, essv12508959, essv12508956, essv12508962 | Samples | HG02481, HG03548, HG03295, NA20356, NA20317, HG03225, HG03073, NA20318, HG03085, HG03046, HG03240 | Known Genes | | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3610429
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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