Variant DetailsVariant: essv11855Internal ID | 9609064 | Landmark | | Location Information | | Cytoband | 10q23.2 | Allele length | Assembly | Allele length | hg38 | 325848 | hg19 | 325848 | hg18 | 325848 | hg17 | 325848 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2758234 | Supporting Variants | | Samples | NA19221 | Known Genes | ADIRF, AGAP11, FAM25A, FAM35A, GLUD1, NUTM2A, NUTM2A-AS1 | 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) | essv11855
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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