Variant DetailsVariant: nsv10824Internal ID | 15499101 | Landmark | | Location Information | | Cytoband | 6p21.32 | Allele length | Assembly | Allele length | hg38 | 65891 | hg19 | 65891 | hg18 | 65890 | hg17 | 65890 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv14916, nssv15582, nssv14235, nssv16454, nssv14197, nssv15249, nssv14643, nssv16131, nssv14034 | Samples | NA18502, NA11830, NA18860, NA07048, NA18975, NA10863, NA18537, NA18517, NA12740 | 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) | nsv10824
| Frequency | Sample Size | 31 | Observed Gain | 5 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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