Variant DetailsVariant: nsv9179 | Internal ID | 15847091 | | Landmark | | | Location Information | | | Cytoband | 15q11.1 | | Allele length | | Assembly | Allele length | | hg38 | 2342212 | | hg19 | 2475760 | | hg18 | 1767110 | | hg17 | 1767110 |
| | Variant Type | CNV gain+loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | nssv27007, nssv21216, nssv22299, nssv25295, nssv20122, nssv19931, nssv26914, nssv22628, nssv21114, nssv22949, nssv21566, nssv21895, nssv20612, nssv21530, nssv22389, nssv22139, nssv27047, nssv26947, nssv24917, nssv21618, nssv21174, nssv19180, nssv21865, nssv24942, nssv24116, nssv25195, nssv24978, nssv24071, nssv21036, nssv26925, nssv21483, nssv21724, nssv25575, nssv21476, nssv20702, nssv19120, nssv21536, nssv23140, nssv22155, nssv26936, nssv25598, nssv19841, nssv21186, nssv24844, nssv25040, nssv21596, nssv20994, nssv21326, nssv24928, nssv22479, nssv19210, nssv26997, nssv25403, nssv25245, nssv25003, nssv25529, nssv22862, nssv20492, nssv19871, nssv22775, nssv19781, nssv25506, nssv22716, nssv21246, nssv21144, nssv22891, nssv21805, nssv21363, nssv22598, nssv22920, nssv22329, nssv22215, nssv22127, nssv23280, nssv22359, nssv24812, nssv19150, nssv23196, nssv20152, nssv25270, nssv25090, nssv24848, nssv22568, nssv22269, nssv21466, nssv23960, nssv19639, nssv19270, nssv25552, nssv24873, nssv21470, nssv20182, nssv21126, nssv24044, nssv24017, nssv22477, nssv21560, nssv20032, nssv22658, nssv23168, nssv21784, nssv21506, nssv19901, nssv19669, nssv23252, nssv25220, nssv22199, nssv21204, nssv20672, nssv19549, nssv19060, nssv21513, nssv23224, nssv24862, nssv25015, nssv21453, nssv19811, nssv21376, nssv24953, nssv21708, nssv21386, nssv20062, nssv21346, nssv20762, nssv19579, nssv20212, nssv26987, nssv19961, nssv25621, nssv19519, nssv20552, nssv21844, nssv21738, nssv24837, nssv22509, nssv25320, nssv22833, nssv19609, nssv22157, nssv21356, nssv21096, nssv21835, nssv26977, nssv25140, nssv22169, nssv21054, nssv20462, nssv22187, nssv22447, nssv26967, nssv25428, nssv21678, nssv25028, nssv20582, nssv21814, nssv25065, nssv19240, nssv25115, nssv20642, nssv22537, nssv21904, nssv19595, nssv22804, nssv22687, nssv20522, nssv22185, nssv22978, nssv22507, nssv21496, nssv25666, nssv23308, nssv21874, nssv21024, nssv21156, nssv26957, nssv25644, nssv25483, nssv22449, nssv21798, nssv21648, nssv21500 | | Samples | NA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552 | | Known Genes | CHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3 | | Method | Oligo aCGH | | Analysis | Statistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2 | | Platform | Agilent-015686 Custom Human 244K CGH Microarray | | Comments | | | Reference | Perry_et_al_2008 | | Pubmed ID | 18304495 | | Accession Number(s) | nsv9179
| | Frequency | | Sample Size | 31 | | Observed Gain | 20 | | Observed Loss | 25 | | Observed Complex | 0 | | Frequency | n/a |
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