Variant DetailsVariant: esv2668092 Internal ID | 9587511 | Landmark | | Location Information | | Cytoband | 14q32.11 | Allele length | Assembly | Allele length | hg38 | 798 | hg19 | 798 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5569418, essv6329819, essv5579394, essv6158328, essv6488878, essv5990547, essv6198032, essv6421452, essv5874267, essv6106141, essv5988882, essv5965337, essv6505382, essv5763808, essv6333071, essv6228298, essv5546071, essv5538599, essv5985672, essv6289821, essv6408138, essv6247382, essv6542810, essv6222269, essv6008094, essv5908890, essv5588438, essv6406885, essv5934842, essv6060918, essv5802085, essv5768764, essv5808510, essv5876236, essv5812982, essv5874941, essv6057403, essv6133942, essv6500013, essv6596592, essv6334248, essv5902423, essv5641973, essv5929819, essv5862722, essv5931472, essv5646128, essv6466061, essv6408954, essv5804141, essv6074667, essv6184295, essv5498205, essv5851121, essv6088101, essv6592782, essv6329015, essv5690148, essv5682674, essv5703619, essv5668065, essv6524984, essv6334117, essv5504733, essv5855318, essv6548494, essv6128346, essv6094636, essv5406652, essv5624474, essv5962329, essv5627113, essv5549745, essv6462019, essv6025566, essv6090190, essv5992523, essv5976641, essv5930989, essv6171203, essv6032478, essv5668194, essv5645685, essv5475097, essv6030595, essv6205985, essv5892925, essv5690060, essv6219737, essv5857423, essv5748745, essv5629788, essv6329248, essv5966213, essv5775310, essv5679656, essv6217924, essv6235746, essv6543164, essv6524690 | Samples | HG01441, NA19058, NA19055, NA18947, NA11829, NA19066, NA18980, NA18999, NA19057, NA18596, NA18959, NA18606, NA19067, HG00693, NA18988, NA18967, NA19068, NA19373, NA19076, NA19005, NA18944, NA18940, HG01070, NA18982, HG01492, NA18960, NA18942, NA19062, HG01354, NA19088, NA19054, NA19384, NA18964, NA19079, NA18949, NA18977, NA19075, NA18986, NA19087, NA19002, NA18990, NA18985, NA18975, NA18973, NA19007, HG00154, NA18951, NA19082, HG01171, NA19070, NA19056, NA19077, NA19462, NA18956, NA19081, NA18637, NA18910, NA18976, NA18948, NA18981, NA19064, NA19000, NA19084, NA19059, NA19009, NA18963, NA18536, NA18945, NA19012, NA18974, NA18953, HG01148, NA19003, NA18961, NA18952, HG00353, NA19072, NA18950, NA18941, NA19380, NA19010, NA19083, NA18943, NA19085, NA19078, NA18971, NA19060, NA18987, NA19080, NA18972, NA18983, NA18984, NA18989, NA19755, NA19004, NA18968, NA19063, NA19065, NA19074, NA18965 | Known Genes | FOXN3 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2668092
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 100 | Observed Complex | 0 | Frequency | n/a |
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