Variant DetailsVariant: esv2721887 Internal ID | 9956185 | Landmark | | Location Information | | Cytoband | 2q37.3 | Allele length | Assembly | Allele length | hg38 | 336 | hg19 | 336 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6864573, essv6880773, essv6853992, essv6686553, essv6878013, essv6962355, essv6669769, essv6892751, essv6833032, essv6859788, essv6825518, essv6906628, essv6793802, essv6817171, essv6872096, essv6973281, essv6797980, essv6889438, essv6848198, essv6718614 | Samples | SSM071, SSM027, SSM011, SSM087, SSM097, SSM093, SSM088, SSM029, SSM089, SSM035, SSM094, SSM031, SSM044, SSM014, SSM072, SSM082, SSM078, SSM080, SSM091, SSM098 | Known Genes | NDUFA10 | 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) | esv2721887
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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