Variant DetailsVariant: esv3641605 Internal ID | 6681690 | Landmark | | Location Information | | Cytoband | 18p11.31 | Allele length | Assembly | Allele length | hg38 | 2816 | hg19 | 2816 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15779913, essv15779972, essv15779888, essv15779932, essv15779927, essv15779915, essv15779920, essv15779971, essv15779902, essv15779944, essv15779961, essv15779914, essv15779895, essv15779878, essv15779937, essv15779957, essv15779877, essv15779943, essv15779951, essv15779926, essv15779899, essv15779924, essv15779938, essv15779934, essv15779950, essv15779919, essv15779966, essv15779968, essv15779947, essv15779946, essv15779965, essv15779905, essv15779964, essv15779942, essv15779901, essv15779886, essv15779956, essv15779876, essv15779960, essv15779906, essv15779885, essv15779958, essv15779918, essv15779896, essv15779917, essv15779875, essv15779973, essv15779907, essv15779912, essv15779936, essv15779954, essv15779935, essv15779910, essv15779898, essv15779949, essv15779911, essv15779891, essv15779969, essv15779887, essv15779941, essv15779939, essv15779962, essv15779880, essv15779909, essv15779928, essv15779922, essv15779931, essv15779894, essv15779890, essv15779929, essv15779953, essv15779879, essv15779904, essv15779963, essv15779889, essv15779908, essv15779884, essv15779967, essv15779955, essv15779923, essv15779930, essv15779925, essv15779883, essv15779970, essv15779872, essv15779874, essv15779933, essv15779948, essv15779900, essv15779873, essv15779897, essv15779882, essv15779945, essv15779881, essv15779916, essv15779952, essv15779940, essv15779893, essv15779921, essv15779959, essv15779892, essv15779903 | Samples | HG00881, HG00650, HG02250, HG02072, NA18621, NA18592, HG01855, NA18565, HG02035, NA18603, HG02017, HG03295, HG02384, NA18519, HG03770, HG02105, HG00689, NA18619, NA18993, NA18558, HG01599, HG00634, NA18942, NA18574, HG00867, HG02512, HG01813, HG02389, NA19024, NA19075, NA18748, HG00422, NA19087, HG04238, HG01440, HG02190, HG03380, HG02138, HG00406, NA19189, NA18990, NA18954, NA18539, NA18645, NA18614, HG02047, NA18747, HG01841, NA19091, HG00982, HG01797, NA19006, HG02678, NA19455, HG02322, HG01845, NA18976, NA18534, HG02364, HG01392, HG03713, HG02121, HG02884, HG01842, NA19225, NA18634, HG00445, HG01812, HG00611, NA19440, NA18543, HG00565, NA19072, NA18950, HG01800, HG01958, HG02314, NA19010, NA18992, HG00473, NA19439, NA19310, HG01260, NA18643, NA19083, HG00662, HG01862, HG02379, HG00513, HG01556, HG02032, NA18994, HG02396, HG01085, NA19213, HG01863, HG04161, HG02351, NA18740, NA18622, NA18965, HG01926 | Known Genes | DLGAP1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3641605
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 102 | Observed Complex | 0 | Frequency | n/a |
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