Variant DetailsVariant: essv5161354Internal ID | 7906068 | Landmark | | Location Information | | Cytoband | 17p13.3 | Allele length | Assembly | Allele length | hg38 | 902390 | hg19 | 955839 | hg18 | 902589 | hg17 | 902589 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2422420 | Supporting Variants | | Samples | ND01666 | Known Genes | ABR, C17orf97, DBIL5P, FAM101B, FAM57A, GEMIN4, GLOD4, LOC100506388, MIR3183, NXN, RNMTL1, RPH3AL, TIMM22, VPS53 | Method | SNP array | Analysis | log R ratio and B allele frequency. | Platform | Not specified | Comments | | Reference | Simon-Sanchez_et_al_2007 | Pubmed ID | 17116639 | Accession Number(s) | essv5161354
| Frequency | Sample Size | 181 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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