Variant DetailsVariant: esv2422397Internal ID | 7906494 | Landmark | | Location Information | | Cytoband | 4p14 | Allele length | Assembly | Allele length | hg38 | 221787 | hg19 | 221787 | hg18 | 221787 | hg17 | 221787 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5161495 | Samples | ND01701 | Known Genes | LOC344967, PDS5A | 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) | esv2422397
| Frequency | Sample Size | 181 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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