Variant DetailsVariant: nsv514477Internal ID | 15466163 | Landmark | | Location Information | | Cytoband | 8p22 | Allele length | Assembly | Allele length | hg38 | 24199 | hg19 | 24199 | hg18 | 24199 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2955059, nssv2955058, nssv2955061, nssv2955060 | Samples | NA21399, NA10863, NA12234, NA12766 | Known Genes | TUSC3 | 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) | nsv514477
| Frequency | Sample Size | 2366 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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