Variant DetailsVariant: esv2673884 Internal ID | 9593303 | Landmark | | Location Information | | Cytoband | 20q12 | Allele length | Assembly | Allele length | hg38 | 289 | hg19 | 289 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5711661, essv5614405, essv5970796, essv5590535, essv6176606, essv5520122, essv6400436, essv6135386, essv5450597, essv5902194, essv5897571, essv5848074, essv6041293, essv6002102, essv6260533, essv5618351, essv5870220, essv5517846, essv6242499, essv5478255, essv6449366, essv6361606, essv5900394, essv5765496, essv6466097, essv5551367, essv5479772, essv6454539, essv6342103, essv6576644, essv6156560, essv5744695, essv5553250, essv5483010, essv6171020, essv6192537, essv6018520, essv5733430, essv5844288, essv5709231, essv6247017, essv6423572, essv5633889, essv6533791, essv5546437, essv6098334, essv5915575, essv5967980, essv5670198, essv6138487, essv6037171, essv6239135, essv5487573, essv5804992, essv5871127, essv6072833, essv5644670, essv5432785, essv6563721, essv6401165, essv5564940, essv5728386, essv6195085, essv5540663, essv6027719, essv5687119, essv5643611, essv6540028, essv6287121, essv5946278, essv5785058, essv5927056, essv5520682, essv5722378, essv6586114, essv6232647, essv5802868, essv5771129, essv6337631, essv6066222, essv5907894, essv5740765, essv6227348, essv6539209 | Samples | HG01441, NA19703, HG00536, NA18924, HG00142, HG00361, HG00524, HG01052, NA18565, HG01079, NA19704, HG01188, NA20531, NA19359, NA20294, NA19819, NA18504, HG00261, NA12399, HG01140, HG00327, NA19446, NA19396, HG00138, NA18519, NA20317, NA19197, HG00369, NA19384, NA18964, HG00243, HG00512, HG00139, NA18868, NA20340, NA19372, NA19385, HG01440, NA19189, NA18990, NA19445, NA20127, NA19985, NA18867, HG00530, HG00183, HG01171, NA19707, NA19403, NA19391, NA19327, HG00740, HG01047, HG00324, HG00284, NA19774, HG01497, NA20282, NA19625, NA19436, NA19375, NA19390, NA20276, NA20520, HG01375, NA19311, HG01108, HG00269, HG00125, NA20341, NA19818, NA19376, NA19398, NA19328, HG00312, HG00342, HG00267, NA20289, HG00310, HG00280, NA19213, NA20503, NA19312, NA19463 | Known Genes | ZHX3 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2673884
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 84 | Observed Complex | 0 | Frequency | n/a |
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