Variant DetailsVariant: essv8936Internal ID | 9631013 | Landmark | | Location Information | | Cytoband | 2q37.1 | Allele length | Assembly | Allele length | hg38 | 296843 | hg19 | 296842 | hg18 | 296842 | hg17 | 296842 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2757849 | Supporting Variants | | Samples | NA19200 | Known Genes | COPS7B, DIS3L2, MIR1244-1, MIR1244-2, MIR1244-3, MIR1471, NPPC, PDE6D, PTMA | 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) | essv8936
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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