Variant DetailsVariant: nsv517155Internal ID | 15097762 | Landmark | | Location Information | | Cytoband | 3q25.1 | Allele length | Assembly | Allele length | hg38 | 35785 | hg19 | 35785 | hg18 | 35785 | hg17 | 35785 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv665692, nssv670027, nssv665549, nssv660490, nssv658351, nssv653926, nssv668991, nssv653888, nssv659090, nssv656462, nssv679762, nssv663926, nssv670149, nssv682732, nssv678031, nssv658456, nssv681567, nssv665336, nssv680976, nssv685121, nssv684424, nssv653372, nssv663219, nssv682151, nssv667901, nssv662629, nssv654575, nssv682205, nssv662124, nssv678327, nssv674220, nssv663106, nssv693150 | Samples | | Known Genes | AADAC, MIR548H2 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517155
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 33 | Observed Complex | 0 | Frequency | n/a |
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