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Copy number variant probe: cnvi0070164

Variation class

CNV_PROBE(SO:0000051)

Source

Illumina_Human660W-quad - Variants from the Illumina Human 660W-Quad whole genome SNP genotyping chip designed for association studies

Location

Chromosome 11:72810 (forward strand) | View in location tab

Explore this SV

Graphical neighbourhood region
Consequences (e.g. missense) (Not available)
Sample level variant data used to define the structural variant (Not available)
Diseases and traits (Not available)

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CNV probe displays