Variant DetailsVariant: nssv2932624Internal ID | 15251038 | Landmark | | Location Information | | Cytoband | 6p21.32 | Allele length | Assembly | Allele length | hg38 | 5513 | hg19 | 5513 | hg18 | 5513 |
| Variant Type | CNV gain | Copy Number | 3 | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv515035 | Supporting Variants | | Samples | NA07435 | Known Genes | C4A, C4B, C4B_2 | Method | Oligo aCGH | Analysis | ADM2 threshold = 5 | Platform | Agilent Eichler Human CNP 180K v3.0 | Comments | | Reference | Campbell_et_al_2011 | Pubmed ID | 21397061 | Accession Number(s) | nssv2932624
| Frequency | Sample Size | 2366 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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