Variant DetailsVariant: esv2743903Internal ID | 9978187 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 278 | hg19 | 311 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6912400, essv6763261, essv6953022, essv6856896, essv6831117, essv6795834, essv6709330, essv6695348, essv6716601 | Samples | SSM071, SSM087, SSM041, SSM062, SSM081, SSM015, SSM037, SSM025, SSM043 | Known Genes | | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2743903
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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