Variant DetailsVariant: essv14108Internal ID | 9611568 | Landmark | | Location Information | | Cytoband | 7p22.3 | Allele length | Assembly | Allele length | hg38 | 490853 | hg19 | 490853 | hg18 | 490853 | hg17 | 490853 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2758099 | Supporting Variants | | Samples | NA18861 | Known Genes | INTS1, MAFK, MICALL2, PSMG3, PSMG3-AS1, TFAMP1, TMEM184A, UNCX, ZFAND2A | 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) | essv14108
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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