Variant DetailsVariant: essv3478Internal ID | 9624949 | Landmark | | Location Information | | Cytoband | 16p12.3 | Allele length | Assembly | Allele length | hg38 | 817244 | hg19 | 734709 | hg18 | 734709 | hg17 | 734709 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2758413 | Supporting Variants | | Samples | NA18992 | Known Genes | ABCC6P1, ARL6IP1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8, RPS15A, SMG1 | 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) | essv3478
| Frequency | Sample Size | 270 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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