Variant DetailsVariant: esv2422398Internal ID | 7906495 | Landmark | | Location Information | | Cytoband | 20q13.33 | Allele length | Assembly | Allele length | hg38 | 466208 | hg19 | 522504 | hg18 | 559554 | hg17 | 559554 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5161340 | Samples | ND01424 | Known Genes | ADRM1, C20orf166, C20orf166-AS1, CABLES2, GATA5, HRH3, LAMA5, LOC100127888, MIR1-1, MIR133A2, MIR4758, OSBPL2, RBBP8NL, RPS21, SLCO4A1 | 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) | esv2422398
| Frequency | Sample Size | 181 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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