Variant DetailsVariant: esv2665399![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg38/?name=chr1:45517815..45517911;width=800;overview=1) Internal ID | 9584818 | Landmark | | Location Information | | Cytoband | 1p34.1 | Allele length | Assembly | Allele length | hg38 | 97 | hg19 | 97 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6357745, essv5415381, essv6474979, essv5493372, essv5940814, essv6442783, essv5444094, essv6027874, essv5846014, essv6434040, essv5795500, essv5771757, essv6004628, essv5931180, essv6048592, essv6359849, essv6368407, essv6534166, essv5424962, essv5416347, essv6424655, essv5518594, essv5594186, essv6004723, essv6020515, essv6321479, essv6163197, essv6222718, essv6065485, essv6157053, essv5520867, essv5578441, essv6561270, essv6565445, essv5560844, essv5904607, essv6502756, essv5609027, essv5985920, essv6171252, essv6423857, essv6062192, essv5889407, essv6044866, essv5650897, essv5742154, essv6373353, essv6362642, essv5958537, essv6303639, essv5635715, essv5856784, essv6134248, essv5689009, essv6565005, essv5873219, essv6263842, essv6168533, essv5445839, essv5898824, essv5620233, essv5827803, essv5605624, essv6430177, essv6066844, essv6138218, essv5722832, essv5931653, essv6114117, essv5519851, essv6492148, essv6129913, essv5623640, essv5499702, essv6125446, essv6486543, essv5729321, essv6573960, essv5849975, essv5700874, essv5404656, essv5703078, essv6458326, essv6417312 | Samples | NA12717, HG00442, NA11995, NA12414, HG01374, HG00699, NA19777, NA18530, NA19190, NA18870, NA18510, NA07357, NA18602, NA19107, HG01350, NA18940, NA18519, HG01351, NA18982, NA18942, NA18916, HG00346, NA18571, NA12287, NA19138, HG00311, NA18611, NA19404, NA12282, HG00335, NA19087, NA18990, NA18557, HG00260, NA10847, HG01353, HG00313, HG00137, HG00190, HG00475, HG00583, HG01498, HG00500, NA20126, NA18572, NA19654, HG00324, HG01073, NA19114, NA11919, NA19084, HG00404, NA20581, HG00276, HG00146, NA18963, NA18523, NA12778, NA18945, NA18542, NA19440, NA11881, NA18961, HG00375, HG00357, NA18941, NA19773, HG00308, HG00473, NA19428, HG00319, NA19085, HG00125, HG00111, NA19785, NA18609, HG00310, HG00252, NA19661, NA18612, NA18622, HG00553, NA18562, NA18577 | Known Genes | PRDX1 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2665399
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 84 | Observed Complex | 0 | Frequency | n/a |
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