Variant DetailsVariant: esv2658394 | Internal ID | 9924499 | | Landmark | | | Location Information | | | Cytoband | 12q22 | | Allele length | | Assembly | Allele length | | hg38 | 877 | | hg19 | 877 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv5717027, essv6476710, essv6357863, essv6233580, essv5732427, essv5422905, essv5411148, essv6316736, essv6067796, essv6153291, essv5875053, essv5757266, essv6410850, essv6100088, essv5724797, essv6496027, essv5534276, essv5473311, essv6416205, essv6142542, essv5609438, essv6449153, essv5710874, essv5492189, essv6291602, essv6463273, essv5850823, essv6476211, essv5577546, essv5688542, essv6578521, essv6514922, essv6036521, essv5712860, essv5535256, essv5600101, essv6313498, essv6387642, essv5850786, essv6327604, essv5890524, essv5697022, essv6336362, essv6115881, essv5409435, essv5467494, essv6530733, essv6437342, essv5604398, essv6276844, essv6271642, essv5872809, essv5795036, essv5572609, essv6117647, essv5899329, essv6540227, essv5918278, essv5868459, essv5648770, essv5948200, essv6017657, essv6355636, essv5430422, essv6165179, essv5628405, essv5927448, essv5777152, essv5432734, essv5453708, essv6373686, essv5585058, essv6079538, essv5474228, essv6228135, essv6168070, essv6261475, essv5489880, essv5852824, essv5471207, essv5916414, essv6258253, essv5676857, essv5646647, essv5529804, essv5569087, essv5693097, essv6455612, essv6115414, essv5693340, essv6130716, essv6351892, essv6461960, essv5878341, essv5896662, essv5533867, essv6364093, essv5653121, essv5786811, essv5677439, essv6512848, essv6415261, essv6405450, essv5940702, essv5466914, essv6334976, essv6256793, essv6483088, essv6097964, essv6011520, essv5890639, essv5496593, essv5556121, essv5404876, essv5628771, essv5675128, essv6565364, essv6288779, essv5631203, essv5784315 | | Samples | NA19055, NA18621, NA19664, NA19066, NA18980, NA11920, HG01188, NA20816, NA18999, HG00244, HG00181, HG00103, NA18596, HG01456, NA12058, HG00179, HG01518, NA20771, NA18602, HG01522, HG00693, NA18988, NA19746, NA19076, NA18944, NA18550, HG01366, NA18597, NA20798, NA18982, NA07048, NA11918, NA19054, NA19782, NA18964, HG00537, HG00311, HG00590, HG00139, HG01067, NA19731, HG00534, NA19087, HG00309, NA18557, NA20757, NA20533, NA20515, NA20753, HG00464, NA19007, HG01353, NA18951, NA20800, NA19070, NA19056, HG01384, NA12003, HG00701, NA19717, NA19788, NA18910, NA18948, HG00239, HG00708, NA19064, HG01094, HG00651, NA19000, HG00250, NA19655, NA11894, HG00117, NA19059, NA19761, NA20534, NA18945, NA18953, NA19003, NA18542, NA18535, HG00265, NA18961, NA18952, NA19747, NA19072, NA18950, HG00580, NA19732, NA19773, NA20785, NA19010, NA19835, HG00473, NA20778, HG01494, NA19083, NA20797, NA19783, NA18610, NA20341, HG00312, NA19060, NA19716, HG01055, HG00280, NA19726, NA19780, NA19661, NA18989, NA19004, HG01125, HG00171, HG00345, NA18623, NA20585, NA19063, NA19065, NA18577, NA20772 | | Known Genes | MRPL42 | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | High quality site | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2658394
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 120 | | Observed Complex | 0 | | Frequency | n/a |
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