Variant DetailsVariant: nsv9686 | Internal ID | 15500912 | | Landmark | | | Location Information | | | Cytoband | 19p12 | | Allele length | | Assembly | Allele length | | hg38 | 664297 | | hg19 | 664297 | | hg18 | 664297 | | hg17 | 664297 |
| | Variant Type | CNV gain+loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | nssv24686, nssv25292, nssv24741, nssv24637, nssv22001, nssv24146, nssv26106, nssv24921, nssv27708, nssv24971, nssv26811, nssv26844, nssv24109, nssv24172, nssv24635, nssv21730, nssv26781, nssv26833, nssv24985, nssv24661, nssv21545, nssv26822, nssv24712, nssv21790, nssv25344, nssv26803, nssv24946, nssv24689, nssv24663, nssv23871, nssv27440, nssv27422, nssv27341, nssv27715, nssv27448, nssv24120, nssv27359, nssv25281, nssv25746, nssv24170, nssv23925, nssv25010, nssv28459, nssv25319, nssv25768, nssv24222, nssv25306, nssv22219, nssv27470, nssv25273, nssv27474, nssv24196, nssv27462, nssv28460, nssv26800, nssv27454, nssv27350, nssv22189, nssv27456, nssv25317, nssv26792, nssv21971, nssv28458, nssv26476, nssv23898, nssv25694, nssv21820, nssv24952, nssv23640, nssv24715, nssv24927, nssv27466, nssv21700, nssv27431, nssv26814 | | 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 | LOC100132815, ZNF724P, ZNF728, ZNF730, ZNF91 | | 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) | nsv9686
| | Frequency | | Sample Size | 31 | | Observed Gain | 30 | | Observed Loss | 15 | | Observed Complex | 0 | | Frequency | n/a |
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