Variant DetailsVariant: esv3619835 Internal ID | 6660021 | Landmark | | Location Information | | Cytoband | 9p22.2 | Allele length | Assembly | Allele length | hg38 | 12430 | hg19 | 12430 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13411946, essv13411926, essv13411956, essv13411942, essv13411943, essv13411931, essv13411949, essv13411951, essv13411937, essv13411933, essv13411945, essv13411925, essv13411950, essv13411932, essv13411944, essv13411936, essv13411948, essv13411928, essv13411929, essv13411941, essv13411927, essv13411924, essv13411958, essv13411947, essv13411930, essv13411935, essv13411960, essv13411952, essv13411955, essv13411939, essv13411953, essv13411940, essv13411934, essv13411938, essv13411954, essv13411957, essv13411959 | Samples | HG02610, NA19397, HG03548, NA19914, NA19378, HG03517, HG02624, HG02895, HG03074, NA18519, HG02703, HG03556, NA19317, HG02502, NA18539, HG02429, NA18856, HG01101, NA19338, HG03046, HG02896, HG03064, HG03367, HG03689, NA20281, NA18501, HG03060, HG02768, HG02676, NA18873, HG03077, HG03162, NA19430, NA19129, HG02643, HG03303, HG02760 | Known Genes | CNTLN | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3619835
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 37 | Observed Complex | 0 | Frequency | n/a |
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