Variant DetailsVariant: esv2743889Internal ID | 9978173 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg19 | 291 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6866882, essv6672841, essv6850867, essv6771876, essv6904727, essv6746678, essv6831115, essv6706033, essv6965460, essv6749530, essv6720501, essv6775537, essv6842260, essv6823431, essv6927759, essv6907274, essv6833421 | Samples | SSM027, SSM079, SSM065, SSM013, SSM002, SSM084, SSM089, SSM019, SSM031, SSM044, SSM086, SSM066, SSM081, SSM040, SSM010, SSM055, SSM056 | Known Genes | MUC2 | 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) | esv2743889
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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