Variant DetailsVariant: nsv8792 Internal ID | 15500018 | Landmark | | Location Information | | Cytoband | 11p15.3 | Allele length | Assembly | Allele length | hg38 | 1915 | hg19 | 1915 | hg18 | 1915 | hg17 | 1915 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv20677, nssv19626, nssv22906, nssv18962, nssv22063, nssv19905, nssv22604, nssv20035, nssv19606, nssv20878, nssv20648, nssv20129, nssv23415, nssv19074, nssv18199, nssv22171, nssv25081, nssv19556, nssv20379, nssv19923, nssv17860, nssv22735, nssv18011, nssv19730, nssv19894, nssv18245 | Samples | NA11830, NA18980, NA07029, NA18504, NA12155, NA12802, NA18860, NA07048, NA10839, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552 | Known Genes | USP47 | 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) | nsv8792
| Frequency | Sample Size | 31 | Observed Gain | 25 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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