Variant DetailsVariant: essv7126Internal ID | 9629003 | Landmark | | Location Information | | Cytoband | 22q11.21 | Allele length | Assembly | Allele length | hg38 | 1005172 | hg19 | 509919 | hg18 | 509919 | hg17 | 509919 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2758535 | Supporting Variants | | Samples | NA18537 | Known Genes | DGCR10, DGCR11, DGCR2, DGCR5, DGCR6, DGCR9, GGT3P, PEX26, PRODH, TUBA8, USP18 | 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) | essv7126
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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