Variant DetailsVariant: nsv8784 Internal ID | 15500010 | Landmark | | Location Information | | Cytoband | 11p15.4 | Allele length | Assembly | Allele length | hg38 | 25296 | hg19 | 25296 | hg18 | 25296 | hg17 | 25296 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv22051, nssv20039, nssv17921, nssv22819, nssv19546, nssv17770, nssv19670, nssv18142, nssv20617, nssv25031, nssv18932, nssv19566, nssv22706, nssv20848, nssv23301, nssv19014, nssv19878, nssv20349, nssv18139, nssv20618, nssv19834, nssv22302, nssv22574, nssv18215, nssv19815, nssv22033, nssv19526, nssv20207, nssv19863, nssv19945 | 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 | OR52N1, OR52N5 | 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) | nsv8784
| Frequency | Sample Size | 31 | Observed Gain | 29 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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