Variant DetailsVariant: esv2758620 Internal ID | 9634079 | Landmark | | Location Information | | Cytoband | 8p21.3 | Allele length | Assembly | Allele length | hg38 | 2578564 | hg19 | 2578566 | hg18 | 2590231 | hg17 | 2590231 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | esv2759604 | Supporting Variants | essv1932, essv19243 | Samples | NA18959, NA10838 | Known Genes | BIN3, BIN3-IT1, BMP1, C8orf58, CCAR2, CHMP7, DMTN, DOK2, EGR3, FAM160B2, FGF17, GFRA2, HR, LGI3, LOC101929172, LOC254896, LOC286059, LOC286114, LOC389641, MIR320A, NPM2, NUDT18, PDLIM2, PEBP4, PHYHIP, PIWIL2, POLR3D, PPP3CC, REEP4, RHOBTB2, SFTPC, SLC39A14, SORBS3, TNFRSF10A, TNFRSF10B, TNFRSF10C, TNFRSF10D, XPO7 | 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) | esv2758620
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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