Variant DetailsVariant: nsv8827Internal ID | 15500053 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 101423 | hg19 | 101423 | hg18 | 101423 | hg17 | 101423 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv18040, nssv19836, nssv20118, nssv18395, nssv18352, nssv19736, nssv22632, nssv20145, nssv19876, nssv23667, nssv20275, nssv20447, nssv18281, nssv23725, nssv20134, nssv25286, nssv20013 | Samples | NA18502, NA18980, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA19007, NA10847, NA10863, NA12872, NA19221, NA18537, NA18564, NA18552 | Known Genes | OR4C11, OR4C6, OR4P4, OR4S2 | 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) | nsv8827
| Frequency | Sample Size | 31 | Observed Gain | 1 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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