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 | essv6219220, essv5548385, essv5561374, essv6447114, essv6238976, essv5561102, essv5504296, essv6266528, essv6017309, essv6127552, essv5632767, essv5903244, essv5836663, essv6037863, essv6383040, essv6309204, essv5868356, essv6004776, essv6336066, essv6075752, essv6500405, essv6426915, essv6132535, essv5549639, essv5994441, essv6176199, essv6344359, essv6306348, essv6589041, essv6280806, essv5829450, essv6360628, essv6169697, essv5397015, essv5814116, essv5663384, essv6033599, essv6430010, essv5626817, essv5647499, essv5422608, essv5881819, essv6598130, essv6097763, essv6451067, essv5548372, essv6342010, essv6476139, essv6211348, essv6362119, essv6158999, essv5409547, essv5795894, essv5950828, essv6033177, essv6135808, essv6380149, essv6184730, essv6465139, essv5886033, essv5468278, essv5441047, essv5643297, essv5800213, essv5688289, essv5532200, essv6014276, essv6264976, essv6006112, essv6116104, essv5452401, essv6324400, essv5926176, essv6319493, essv5924212, essv5563662, essv5427877, essv6295967, essv6217051, essv6497234, essv5786935, essv5509631, essv6059653, essv5715973, essv6098709, essv5765081, essv5650825, essv6483252, essv5864032, essv5559324, essv6369005 | Samples | NA20588, HG00650, HG00442, HG01374, NA18603, HG00699, NA18530, NA18606, HG01140, NA18988, HG00327, HG00663, HG00138, HG01350, HG01366, HG01070, HG00589, NA20586, NA18547, HG00346, NA18582, NA18571, HG01083, NA19138, NA18964, NA18611, HG00512, HG00281, HG01069, NA18617, HG00705, NA18986, NA18557, HG00419, NA19789, HG00464, HG01353, HG00137, HG00154, HG01360, NA19077, HG00428, HG00653, HG00657, HG00436, HG00556, HG00584, HG00583, HG00263, HG00619, NA19064, HG00324, HG00284, HG00404, HG00684, NA18532, HG00613, HG00321, NA19009, HG00704, NA18546, NA18632, NA18543, NA18559, NA18564, NA19072, HG00580, NA19010, HG00473, HG00237, HG00319, HG00662, HG00418, NA18615, HG00620, NA19328, NA19078, HG00707, HG00614, HG00111, HG00513, HG00421, HG00656, HG00472, NA18612, NA18549, NA19074, NA18622, HG00437, NA18577, NA18620 | 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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