Variant DetailsVariant: nssv15582Internal ID | 15486037 | Landmark | | Location Information | | Cytoband | 6p21.32 | Allele length | Assembly | Allele length | hg38 | 64194 | hg19 | 64194 | hg18 | 64194 | hg17 | 64194 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv10824 | Supporting Variants | | Samples | NA18502 | Known Genes | C4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB | 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) | nssv15582
| Frequency | Sample Size | 31 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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