Variant DetailsVariant: esv2664023 | Internal ID | 9583442 | | Landmark | | | Location Information | | | Cytoband | 17q25.3 | | Allele length | | Assembly | Allele length | | hg38 | 110 | | hg19 | 110 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv5643297, essv5647499, essv6280806, essv5427877, essv6380149, essv5950828, essv5504296, essv5814116, essv6309204, essv6264976, essv5800213, essv5864032, essv5765081, essv5836663, essv6097763, essv6447114, essv6344359, essv6176199, essv6476139, essv6017309, essv5549639, essv6014276, essv6132535, essv5688289, essv6158999, essv5994441, essv6589041, essv6238976, essv5924212, essv6184730, essv6033177, essv5881819, essv5559324, essv6033599, essv5626817, essv6430010, essv5926176, essv6451067, essv5868356, essv6383040, essv6217051, essv6135808, essv5509631, essv6004776, essv6426915, essv5532200, essv6219220, essv5441047, essv6006112, essv5886033, essv5903244, essv6266528, essv6306348, essv5397015, essv5663384, essv5632767, essv5548385, essv6360628, essv5409547, essv6369005, essv6500405, essv6098709, essv5548372, essv6319493, essv6483252, essv5829450, essv6497234, essv6598130, essv6127552, essv6336066, essv5786935, essv6465139, essv5795894, essv5422608, essv6037863, essv5563662, essv5561374, essv6059653, essv5561102, essv5468278, essv6169697, essv6324400, essv6295967, essv6075752, essv5452401, essv5650825, essv6116104, essv6211348, essv6342010, essv6362119, essv5715973 | | Samples | HG00613, NA18964, HG00619, HG01353, NA18530, HG00418, HG00705, HG00437, HG01083, NA18612, HG00464, NA19072, HG00707, NA18603, HG00657, HG00614, HG00428, NA19010, HG01350, NA18546, NA20588, HG00111, HG00404, HG00319, HG00699, NA18557, NA20586, NA18632, NA19077, HG00154, NA18559, HG00321, HG00556, HG00346, HG01140, HG00472, HG00421, HG00583, NA18622, NA18617, HG00419, NA18547, HG01360, HG00284, HG00237, HG00584, HG00662, HG00436, HG00620, NA18620, HG00653, NA18986, HG00263, HG01069, NA18564, HG00513, NA18988, HG00512, HG01070, NA19074, NA19328, NA19789, HG00589, NA18606, NA18543, NA18582, NA19138, NA19078, HG00650, NA19009, HG00138, HG00663, HG00580, NA18577, NA19064, HG00281, HG00656, HG01366, NA18571, NA18611, HG00324, NA18532, NA18549, HG00442, HG01374, HG00473, HG00137, HG00684, NA18615, HG00704, HG00327 | | Known Genes | OGFOD3 | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2664023
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 91 | | Observed Complex | 0 | | Frequency | n/a |
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