Variant DetailsVariant: nsv574714Internal ID | 16015437 | Landmark | | Location Information | | Cytoband | 17q12 | Allele length | Assembly | Allele length | hg38 | 968554 | hg19 | 968554 | hg18 | 968554 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv869638 | Samples | | Known Genes | ASIC2, C17orf102, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8, TMEM132E | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv574714
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|