Variant DetailsVariant: esv2676825 Internal ID | 9596244 | Landmark | | Location Information | | Cytoband | 13q14.13 | Allele length | Assembly | Allele length | hg38 | 236 | hg19 | 236 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5504080, essv6524570, essv6563831, essv6219429, essv5875868, essv5662488, essv6387446, essv5415246, essv5979151, essv6369538, essv5684861, essv5682921, essv6098712, essv5724884, essv5675069, essv6545961, essv5563261, essv5430023, essv5838693, essv6522465, essv6214893, essv6281042, essv6489189, essv5427243, essv5574483, essv5582181, essv5938815, essv6339561, essv5747448, essv5890886, essv6081443, essv6307987, essv5685783, essv5498296, essv5442654, essv6131105, essv5830033, essv6334143, essv6534574, essv6396216, essv6510965, essv5416903, essv5664899, essv6251580, essv6024828, essv5786822, essv6222020, essv6347156, essv5558524, essv5672283, essv5420279, essv6202290, essv6392544, essv5539833, essv6388957, essv5521956, essv5745632, essv5578133, essv6450664, essv6390767, essv5761460, essv5828192, essv5901825, essv5925029, essv6103488, essv5543448, essv5997039, essv5472147, essv5943112, essv5552922, essv5506987, essv6332758, essv5831643, essv5678173, essv5620784, essv6225373, essv5609833, essv6240969, essv6392729, essv5501736, essv5518950, essv6026634, essv6198901, essv5824755, essv6115878, essv5928649, essv6347907, essv6089516, essv6495496, essv5697206, essv5529992, essv5538908, essv5507497, essv5806383, essv5828739, essv6233449, essv6484153, essv5439357, essv5881898, essv5982137 | Samples | HG00323, HG00613, HG00309, HG00313, HG00252, HG00318, HG00536, HG00607, HG00257, NA18534, NA18530, HG01052, HG00328, HG01055, HG01083, HG00274, HG00310, HG00261, HG01389, HG00463, HG00614, HG01365, HG01492, HG01082, HG00375, HG01174, NA18542, HG01350, NA18546, HG00111, HG00334, HG00335, HG01101, HG00319, HG00253, HG01171, HG00353, HG00256, HG00543, HG00339, HG00346, HG01375, HG00337, HG00140, NA19443, NA18623, HG01048, HG01061, HG00692, HG00315, HG00330, NA18638, HG00338, HG00125, NA18637, HG00276, HG00284, HG01187, NA12830, HG00662, HG00108, HG00268, HG01066, HG00263, HG00672, HG00282, HG01170, HG00249, HG00478, HG00277, HG01080, HG01351, HG00329, HG00512, HG00534, HG01060, HG00236, NA18543, HG01137, HG00590, HG01334, NA18577, HG01390, HG00285, NA19225, NA12546, HG00422, HG01108, HG00693, NA18611, HG00320, HG00275, HG00324, NA18549, HG00137, HG01102, HG00684, HG00143, HG00278, HG00327 | Known Genes | | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2676825
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 100 | Observed Complex | 0 | Frequency | n/a |
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