Variant DetailsVariant: esv2757890Internal ID | 9633349 | Landmark | | Location Information | | Cytoband | 3q22.3 | Allele length | Assembly | Allele length | hg38 | 322047 | hg19 | 322047 | hg18 | 322047 | hg17 | 322047 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | esv2759180 | Supporting Variants | essv7121, essv22152, essv4766, essv4220, essv5310, essv22648, essv152, essv18747, essv22424, essv18370, essv20910, essv6319, essv19388, essv12776, essv18603 | Samples | NA18603, NA12801, NA10857, NA18563, NA12752, NA19120, NA12234, NA18537, NA11840, NA12249, NA10861, NA12874, NA18609, NA18968, NA18620 | Known Genes | A4GNT, ARMC8, CLDN18, DBR1, DZIP1L | 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) | esv2757890
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 15 | Observed Complex | 0 | Frequency | n/a |
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