Variant DetailsVariant: dgv313n27 Internal ID | 20132571 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 152703 | hg19 | 152703 | hg18 | 152703 | hg17 | 152703 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv456932, nsv457046, nsv456995, nsv456931, nsv456967, nsv457032, nsv456933, nsv456987, nsv457059, nsv457020, nsv457024, nsv456948, nsv456984, nsv457058, nsv457014, nsv457034, nsv457069, nsv456940, nsv456981, nsv457021, nsv456962, nsv456990, nsv457016, nsv456951, nsv457040, nsv456957, nsv456973, nsv457038, nsv456970, nsv456955, nsv456977, nsv456986, nsv456939, nsv457003, nsv457023, nsv456954, nsv456936, nsv457050, nsv457000, nsv457067, nsv457022, nsv456972, nsv457061, nsv456966, nsv457009, nsv457028, nsv456975, nsv456944, nsv457036, nsv456982, nsv457070, nsv456929, nsv456950, nsv456958, nsv456956, nsv457056, nsv456938, nsv457012, nsv457007, nsv457051, nsv456942, nsv457055, nsv457013, nsv456991, nsv457043, nsv457005, nsv457047, nsv456960, nsv456959, nsv456993, nsv457045, nsv457064, nsv456988, nsv457062, nsv457001, nsv457042, nsv456976, nsv457057, nsv456961, nsv456978, nsv457006, nsv457065, nsv457027, nsv457039, nsv457060, nsv456928, nsv457017, nsv456964, nsv456949, nsv457048, nsv456998, nsv456994, nsv457033, nsv457044, nsv457029, nsv456953, nsv457002, nsv456971, nsv456983, nsv456935, nsv456979, nsv457004, nsv456937, nsv456989, nsv456945, nsv457054, nsv456943, nsv456980, nsv456926, nsv457035, nsv456947, nsv457053, nsv457031, nsv456968, nsv456934, nsv456927, nsv457015 | Samples | HGDP00544, HGDP00417, 1780854463_A, HGDP00135, NINDS_243, NINDS_116, HGDP00491, 1782681111_A, HGDP00630, HGDP01350, HGDP00814, 1780862547_A, HGDP00794, HGDP00554, HGDP01377, HGDP00772, HGDP01081, HGDP00579, HGDP00870, HGDP00210, 1780862378_A, HGDP01184, 1780854318_A, HGDP00226, HGDP01059, HGDP01254, 1780862126_A, HGDP01237, HGDP00191, 1780854537_A, HGDP01300, 1780862415_A, 1780862355_A, HGDP01283, HGDP00455, 1780862539_A, 1780854023_A, NINDS_199, HGDP00189, 1782681080_A, HGDP01202, NINDS_247, HGDP01403, 1780862460_A, 1782681378_A, NINDS_217, 1780854264_A, HGDP00547, HGDP00298, 1780862424_A, 1780854334_A, HGDP00183, NINDS_60, 1782681275_A, 1780862585_A, HGDP01290, 1780862227_A, HGDP00778, HGDP00556, NINDS_29, NINDS_110, HGDP00100, HGDP01338, HGDP00035, NINDS_226, HGDP00438, 1780854238_A, HGDP00146, 1798860491_A, HGDP01408, HGDP00148, 1780862448_A, HGDP00540, HGDP01348, HGDP00682, HGDP00613, 1780862578_A, HGDP00670, NINDS_114, HGDP00975, 1780862577_A, 1798860565_A, 1780862470_A, HGDP01245, HGDP01318, HGDP00686, HGDP00552, 1788485589_A, HGDP00601, 1780862084_A, HGDP01009, NINDS_85, HGDP00131, HGDP01376, 1780862584_A, 1780862085_A, HGDP01027, HGDP00877, HGDP00070, 1782681142_A, HGDP01029, HGDP01153, HGDP01275, 1782681495_A, NINDS_80, HGDP00412, HGDP00701, 1780862197_A, HGDP00669, NINDS_181, 1780846030_A, 1780854327_A, NINDS_245, HGDP01221, 1780862437_A, HGDP00181, 1780862304_A | Known Genes | GOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2 | Method | SNP array | Analysis | An HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives. | Platform | Not reported | Comments | | Reference | Itsara_et_al_2009 | Pubmed ID | 19166990 | Accession Number(s) | dgv313n27
| Frequency | Sample Size | 1557 | Observed Gain | 0 | Observed Loss | 117 | Observed Complex | 0 | Frequency | n/a |
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