Variant DetailsVariant: esv2677848 Internal ID | 9597267 | Landmark | | Location Information | | Cytoband | 10p12.1 | 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 | essv6235468, essv5859390, essv6064717, essv5772813, essv5406517, essv5814844, essv6283920, essv6546837, essv5543487, essv5478086, essv6024178, essv5854226, essv6385949, essv6003006, essv5546736, essv5493617, essv6144127, essv5749167, essv6183227, essv6536489, essv5629574, essv5807477, essv5869419, essv5542675, essv5473905, essv6188422, essv5864089, essv6105702, essv5799814, essv5514150, essv6139731, essv5755709, essv5625188, essv5521926, essv5904552, essv5783982, essv5674366, essv6283202, essv6362499, essv5663394, essv6093347, essv6116436, essv5680178, essv5496940, essv5470601, essv5976419, essv6182636, essv5629688, essv5702471, essv5601513, essv6277501, essv6274429, essv6261220, essv6570459, essv6442732, essv6376737, essv5831267, essv5536563, essv6241324, essv5556954, essv5797340, essv5672633, essv5845298, essv5963059, essv6110035, essv5791254, essv6197306, essv5611727, essv6546599, essv6050003, essv6100229, essv5875861, essv5833306, essv6380056, essv5453079, essv6365351, essv5449296, essv5829421, essv6013492, essv5982465 | Samples | HG00626, HG00671, NA19066, HG00559, HG00524, NA18561, NA18999, NA18603, NA19057, NA18530, NA19068, NA18944, NA18550, HG01070, HG00272, HG00501, HG01488, NA18567, NA18558, HG00330, NA18547, HG00634, NA18960, NA18942, NA18618, NA18964, HG00537, NA19079, NA18611, HG00512, HG01069, NA18977, HG00325, NA18986, NA18557, NA18985, HG00313, NA18544, HG00560, HG00731, HG00557, HG00657, NA18991, NA18572, NA18534, HG00708, NA19000, NA18626, HG00531, HG00684, HG00613, HG00525, NA18555, HG00704, NA18634, NA18541, NA18576, NA18546, NA18608, NA18953, NA18543, HG00625, HG00580, NA19010, HG00607, NA18943, HG00418, HG00672, HG00513, NA18609, NA18552, NA18983, HG00595, NA18989, NA19063, NA19065, NA18612, NA18549, HG01061, NA18577 | Known Genes | MKX | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2677848
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 80 | Observed Complex | 0 | Frequency | n/a |
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