Variant DetailsVariant: esv3619836 Internal ID | 6660022 | Landmark | | Location Information | | Cytoband | 9p22.2 | Allele length | Assembly | Allele length | hg38 | 6058 | hg19 | 6058 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13412045, essv13411996, essv13411978, essv13411994, essv13411992, essv13412006, essv13412023, essv13411975, essv13412022, essv13412028, essv13412034, essv13412008, essv13411971, essv13412007, essv13411983, essv13412039, essv13412000, essv13411991, essv13412025, essv13412052, essv13412012, essv13411989, essv13411980, essv13412030, essv13412032, essv13412013, essv13411968, essv13412003, essv13411962, essv13412049, essv13412005, essv13412009, essv13412020, essv13411988, essv13412016, essv13411974, essv13411961, essv13411963, essv13412035, essv13412036, essv13411993, essv13412021, essv13412026, essv13412002, essv13412043, essv13412015, essv13411977, essv13411984, essv13412046, essv13412040, essv13411998, essv13411995, essv13412041, essv13411982, essv13411969, essv13412014, essv13411972, essv13411979, essv13411987, essv13411990, essv13412010, essv13411964, essv13412048, essv13411965, essv13412001, essv13411981, essv13412037, essv13412031, essv13411967, essv13412024, essv13412047, essv13411986, essv13412044, essv13412051, essv13412004, essv13411997, essv13411966, essv13412011, essv13412033, essv13412042, essv13412029, essv13411976, essv13411970, essv13412018, essv13411999, essv13412027, essv13411985, essv13412038, essv13412019, essv13412017, essv13411973, essv13412050 | Samples | HG02944, HG02610, HG02250, HG03121, NA19397, HG03548, NA19914, HG03111, NA19378, HG03517, HG03057, HG02798, NA18917, NA20294, HG02624, HG03193, HG02589, HG02536, NA19443, HG02895, HG03074, NA18519, HG02595, HG01816, HG02816, HG02505, HG03520, HG02703, HG00867, HG03556, HG00683, HG01813, NA19317, HG02502, HG02946, NA18864, HG03369, NA18539, HG02164, HG02402, NA19455, HG02108, HG00598, HG03575, HG02508, HG02014, HG03085, HG02429, NA19031, NA18856, HG01101, NA19338, HG02979, HG03046, HG02896, HG02568, HG01811, HG03064, HG02807, HG03461, NA19149, HG03367, NA19749, HG02721, HG03689, HG02923, NA18865, HG02274, HG01108, NA20281, HG03103, NA20357, NA18501, HG02974, HG02938, HG03060, HG01799, HG02768, HG02676, NA18873, HG03077, HG02052, HG03162, HG02353, NA19430, NA19129, HG00628, HG03198, HG02643, HG03303, HG02760, HG00593 | Known Genes | CNTLN | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3619836
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 92 | Observed Complex | 0 | Frequency | n/a |
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