Variant DetailsVariant: esv2725293| Internal ID | 10308929 | | Landmark | | | Location Information | | | Cytoband | 3p14.3 | | Allele length | | Assembly | Allele length | | hg38 | 468 | | hg19 | 468 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6864660, essv6955722, essv6859872, essv6854092, essv6817240, essv6906694, essv6962455, essv6669871, essv6847919 | | Samples | SSM027, SSM087, SSM088, SSM026, SSM089, SSM031, SSM014, SSM086, SSM078 | | 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) | esv2725293
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 9 | | Observed Complex | 0 | | Frequency | n/a |
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