Variant DetailsVariant: esv2660474 Internal ID | 9579893 | Landmark | | Location Information | | Cytoband | 4q21.23 | Allele length | Assembly | Allele length | hg38 | 322 | hg19 | 322 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5540780, essv6291885, essv6194814, essv6177037, essv5494828, essv6132965, essv5474484, essv6212170, essv5663480, essv6385378, essv5908708, essv5673898, essv5960235, essv6095418, essv5990368, essv6404507, essv6429649, essv6448746, essv5877692, essv6560594, essv5627670, essv6078408, essv6256238, essv5490236, essv5612286, essv5879908, essv6445033, essv6033598, essv6545765, essv6523199, essv6056115, essv5435119, essv6546240, essv5821714, essv5992363, essv5835923, essv5670356, essv6141498, essv5941056, essv5914920, essv6190157, essv6137960, essv6399583, essv6268824, essv5617183, essv6574334, essv5585505, essv6020013, essv5565242, essv6097202, essv6185803, essv5588614, essv5524503, essv5988959, essv5427799, essv5642789, essv6396963, essv5421554, essv5994788, essv6200004, essv6582597, essv6459708, essv5829117, essv5781904, essv5554727, essv6442931, essv6345029, essv5970708, essv5688329, essv6032452, essv6557285, essv6069472, essv6372845, essv6010375, essv6399077, essv6232449, essv6104724, essv5455298, essv6077666, essv5902223, essv6012802, essv6138727, essv5961477, essv5833448, essv6204106, essv5434923, essv5434733, essv6551022, essv6434042, essv6412872, essv6251860, essv5732140, essv6062680, essv6539552, essv5832680, essv5403724, essv6067476, essv6371740, essv6150121, essv6423217, essv5820494, essv5813949, essv5990025, essv5686866, essv5493392, essv6432321 | Samples | NA19394, NA12383, NA18502, HG01441, NA19703, NA19397, NA18924, NA18861, NA18508, NA19399, NA19914, NA19704, NA18507, HG01188, NA18917, NA19359, NA19355, NA19393, NA18504, NA19377, NA18870, NA19920, NA19374, NA19396, NA19381, HG01350, NA19379, NA19315, NA19448, NA18595, HG01177, NA18923, NA18916, NA19457, NA19313, NA19138, NA18498, NA19904, HG01110, NA19130, NA19383, NA18874, NA18868, NA20340, NA19372, NA19371, NA19238, NA19901, NA19189, NA18520, NA19239, HG00326, NA18973, NA19921, HG01353, NA19908, NA19657, NA19707, NA18934, HG01095, NA19391, NA18910, NA20344, HG01102, NA19461, NA18499, NA18853, NA19099, NA19338, NA19257, NA19452, NA19225, NA18523, NA19469, NA19395, NA19440, NA19108, NA19147, NA18517, NA20276, NA19712, NA19434, HG00734, NA19444, NA19331, NA19240, NA19311, HG01108, NA20281, NA19360, NA20341, NA19398, HG00259, NA19093, NA20289, NA20786, NA19102, NA19116, NA19711, NA19213, HG01082, NA19312, NA19463, NA18511, NA18522, HG01191 | Known Genes | ARHGAP24 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2660474
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 106 | Observed Complex | 0 | Frequency | n/a |
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