Variant DetailsVariant: essv14854Internal ID | 9612396 | Landmark | | Location Information | | Cytoband | 20q13.33 | Allele length | Assembly | Allele length | hg38 | 274019 | hg19 | 274019 | hg18 | 274019 | hg17 | 274019 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2758526 | Supporting Variants | | Samples | NA18522 | Known Genes | ARFRP1, C20orf195, EEF1A2, GMEB2, HELZ2, KCNQ2, LIME1, PPDPF, PTK6, RTEL1, RTEL1-TNFRSF6B, SLC2A4RG, SRMS, STMN3, TNFRSF6B, ZBTB46, ZGPAT | Method | BAC aCGH | Analysis | Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd). | Platform | Agilent | Comments | | Reference | Redon_et_al_2006 | Pubmed ID | 17122850 | Accession Number(s) | essv14854
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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