Variant DetailsVariant: dgv85n27 Internal ID | 20132343 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 160292 | hg19 | 160292 | hg18 | 160292 | hg17 | 160292 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv467042, nsv466945, nsv466946, nsv466999, nsv467044, nsv466995, nsv467010, nsv467050, nsv467030, nsv467057, nsv466996, nsv466982, nsv467018, nsv467046, nsv466955, nsv466993, nsv466954, nsv466970, nsv466953, nsv467025, nsv467004, nsv466939, nsv467048, nsv466989, nsv466944, nsv466990, nsv466956, nsv466998, nsv466979, nsv467012, nsv467041, nsv467003, nsv467034, nsv467029, nsv466959, nsv467031, nsv467020, nsv466974, nsv467023, nsv466987, nsv466966, nsv467000, nsv467024, nsv466980, nsv467006, nsv467035, nsv467017, nsv466988, nsv466952, nsv466951, nsv467013, nsv466985, nsv466960, nsv466978, nsv467001, nsv466992, nsv466984, nsv466941, nsv467043, nsv467037, nsv466964, nsv466958, nsv467040, nsv466986, nsv466976, nsv467021, nsv467008, nsv467047, nsv467015, nsv467019, nsv466943, nsv467033, nsv466971, nsv467055, nsv467009, nsv466940, nsv466957, nsv466977, nsv466948, nsv466962, nsv466965, nsv467056, nsv467051, nsv466973, nsv466947, nsv467028, nsv467014, nsv466975, nsv466991, nsv466967, nsv467052, nsv467053, nsv466963, nsv466968, nsv467002, nsv466969, nsv466942, nsv466981, nsv467026, nsv467032, nsv467054, nsv466997, nsv467045, nsv467011 | Samples | 1782681076_A, HGDP00157, HGDP00607, HGDP00640, 1782681093_A, HGDP01379, 1780862307_A, HGDP00739, HGDP00127, HGDP00025, HGDP00884, NINDS_243, HGDP00577, HGDP00646, HGDP00654, HGDP00154, HGDP00626, HGDP00888, HGDP01156, HGDP00136, 1780862304_A, HGDP00423, 1780862433_A, 1780862410_A, 1780854039_A, HGDP00677, HGDP00428, 1782681086_A, HGDP00945, HGDP00021, HGDP00886, HGDP00600, 1780854537_A, 1780854464_A, 1780854517_A, HGDP00251, 1782681313_A, HGDP00476, 1787431198_A, HGDP00462, 1780862599_A, 1798860592_A, HGDP00612, 1780862480_A, HGDP00787, 1780862160_A, HGDP00785, HGDP00883, HGDP00526, 1798860565_A, HGDP01332, HGDP00895, HGDP00684, 1780854216_A, HGDP00039, HGDP00108, 1780862252_A, HGDP01296, 1780862360_A, HGDP00254, HGDP01253, HGDP00037, 1780862274_A, HGDP00208, HGDP00226, HGDP01352, HGDP00650, 1780854538_A, HGDP00338, HGDP01359, 1782681296_A, HGDP00644, 1798860084_A, 1780854463_A, HGDP00693, 1780854382_A, HGDP00649, HGDP00731, 1798860191_A, HGDP00143, 1780854393_A, 1798860114_A, HGDP01155, HGDP01248, 1780854441_A, HGDP00901, HGDP00896, HGDP00134, HGDP00445, HGDP00364, HGDP00882, HGDP00625, 1798860569_A, HGDP00189, HGDP01177, 1798860570_A, HGDP00140, HGDP00007, 1780854296_A, 1780862416_A, 1782681117_A, 1787431196_A, 1780854477_A, HGDP00790 | Known Genes | ANTXRL, ANTXRLP1 | 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) | dgv85n27
| Frequency | Sample Size | 1557 | Observed Gain | 104 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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