Variant DetailsVariant: esv3608572 | Internal ID | 6648805 | | Landmark | | | Location Information | | | Cytoband | 6p21.33 | | Allele length | | Assembly | Allele length | | hg38 | 7351 | | hg19 | 7351 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv12263933, essv12263948, essv12263969, essv12263966, essv12263967, essv12263961, essv12263929, essv12263957, essv12263951, essv12263973, essv12263949, essv12263960, essv12263963, essv12263940, essv12263972, essv12263936, essv12263946, essv12263955, essv12263958, essv12263942, essv12263945, essv12263965, essv12263923, essv12263928, essv12263962, essv12263925, essv12263959, essv12263932, essv12263930, essv12263975, essv12263956, essv12263939, essv12263968, essv12263954, essv12263964, essv12263937, essv12263922, essv12263935, essv12263931, essv12263947, essv12263943, essv12263941, essv12263974, essv12263971, essv12263926, essv12263952, essv12263924, essv12263950, essv12263938, essv12263953, essv12263934, essv12263970, essv12263927, essv12263944 | | Samples | HG03690, HG03559, HG02890, HG00542, HG02798, HG03455, HG02888, HG03836, HG03950, NA19005, HG04022, NA18619, HG02374, HG02131, NA20539, HG00335, HG01767, NA18748, HG02571, NA19725, NA18520, NA19456, NA18645, HG02716, HG01139, HG03908, NA18538, HG03787, HG04035, HG03027, HG02121, HG03953, HG02081, NA19338, NA21142, NA21144, HG02220, NA19072, HG03838, HG02837, NA19144, NA18591, HG01798, HG03442, HG01917, HG03066, HG02646, NA21133, HG02679, NA19080, HG03538, HG03470, HG02855, HG01776 | | Known Genes | C2 | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3608572
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 54 | | Observed Complex | 0 | | Frequency | n/a |
|
|