Variant DetailsVariant: esv2676588Internal ID | 9596007 | Landmark | | Location Information | | Cytoband | 22q13.31 | Allele length | Assembly | Allele length | hg38 | 2286 | hg19 | 2286 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv837e199 | Supporting Variants | essv6279687, essv6574239, essv6054346, essv6345154, essv5428510, essv5788186, essv6209316, essv6534811, essv5859094, essv5845213, essv5763516, essv6439116, essv5477664, essv5947164, essv5967259, essv5757441, essv5850259, essv5926322, essv6502353, essv5559148, essv5947516, essv5461730, essv6507705, essv5582445, essv6501648, essv6368674, essv6427038, essv5700977, essv6222417, essv5686062, essv6135599, essv5517449, essv5520959, essv5893364, essv6304493, essv6369001, essv5948803, essv6127586, essv6579682, essv5842094, essv6426961, essv5399880, essv6594190, essv5559520, essv5644297, essv5545285, essv5615428, essv6183266, essv5667471, essv6469626 | Samples | NA18924, NA18861, NA18486, NA18504, NA19190, NA19098, NA19171, NA18489, NA18923, NA19198, NA18498, NA19130, NA18868, NA19235, NA19172, NA19159, NA19189, NA18520, NA19209, NA18867, NA19200, NA19247, NA18934, NA19152, NA18933, NA19236, NA18516, NA18910, NA18871, NA19114, NA18499, NA18856, NA18912, NA19099, NA19257, NA19225, NA18523, NA19160, NA18858, NA18909, NA19144, NA19223, NA19102, NA18873, NA19116, NA19213, NA18505, NA18511, NA18522, NA18487 | Known Genes | PRR5-ARHGAP8 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2676588
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 50 | Observed Complex | 0 | Frequency | n/a |
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