Variant DetailsVariant: esv3618150 Internal ID | 6658345 | Landmark | | Location Information | | Cytoband | 8q22.2 | Allele length | Assembly | Allele length | hg38 | 2619 | hg19 | 2619 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13267377, essv13267355, essv13267370, essv13267348, essv13267354, essv13267358, essv13267344, essv13267371, essv13267362, essv13267350, essv13267368, essv13267345, essv13267379, essv13267369, essv13267349, essv13267351, essv13267364, essv13267365, essv13267356, essv13267373, essv13267347, essv13267353, essv13267367, essv13267374, essv13267378, essv13267372, essv13267346, essv13267342, essv13267360, essv13267343, essv13267361, essv13267359, essv13267376, essv13267366, essv13267363, essv13267357, essv13267352, essv13267380, essv13267375 | Samples | HG03514, NA19701, HG02944, HG03300, HG03115, HG03100, HG03518, NA18870, NA19107, NA19171, HG02549, NA19138, HG02505, HG02281, HG02420, HG03160, HG02334, NA19152, NA19984, HG03291, HG01077, NA18910, NA19042, HG02283, HG03571, NA19225, HG03354, HG03109, NA19436, NA19035, NA19434, HG02308, NA19454, HG02941, NA19117, HG03157, NA19030, NA19153, HG03166 | Known Genes | | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3618150
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 39 | Observed Complex | 0 | Frequency | n/a |
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