Variant DetailsVariant: esv2661577 | Internal ID | 9927682 | | Landmark | | | Location Information | | | Cytoband | 8p23.1 | | Allele length | | Assembly | Allele length | | hg38 | 22548 | | hg19 | 22548 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv1266e199 | | Supporting Variants | essv5686398, essv6234166, essv5397679, essv6351999, essv5582772, essv5457274, essv5963032, essv5929271, essv6253127, essv5810092, essv6441213, essv5647562, essv6380249, essv5868978, essv5883924, essv5555210, essv6499552, essv6587717, essv5699136, essv6081246, essv5966283, essv5843148, essv6187887, essv6222157, essv6403561, essv6497497, essv5702554, essv5921632, essv5905522, essv6204717, essv6369589, essv6259182, essv6424050, essv6139453, essv5674852, essv5643994, essv5518127, essv5972306, essv5592631, essv5436283, essv6426978, essv6504791, essv5434727, essv6400205, essv6449927, essv6180695, essv6553549, essv5613601, essv6550439, essv5562794, essv6264336, essv5640361, essv5899288, essv5494214, essv5482146, essv5813364, essv5719274 | | Samples | NA19058, NA18947, NA19066, NA18980, NA18999, NA19057, NA18959, NA18967, NA19068, NA19076, NA19005, NA18944, NA18940, NA18982, NA18960, NA18942, NA19054, NA19079, NA18949, NA18977, NA18986, NA19087, NA19002, NA18990, NA18985, NA19007, NA18951, NA19082, NA19056, NA18956, NA19081, NA18976, NA18948, NA18981, NA19064, NA19000, NA19084, NA19059, NA19009, NA18945, NA18953, NA19003, NA18961, NA18941, NA19010, NA18943, NA19085, NA19078, NA19060, NA18987, NA19080, NA18972, NA18983, NA18989, NA19063, NA19074, NA18965 | | Known Genes | | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2661577
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 57 | | Observed Complex | 0 | | Frequency | n/a |
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