Variant DetailsVariant: esv2743905Internal ID | 9978189 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 577 | hg19 | 263 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6771880, essv6706036, essv6940122, essv6731925, essv6842259, essv6815295, essv6681406, essv6779264, essv6775541, essv6728146 | Samples | SSM046, SSM065, SSM084, SSM047, SSM067, SSM033, SSM066, SSM040, SSM077, SSM022 | 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) | esv2743905
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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