GEO DataSets

(Submitter supplied) Objectives: Despite recent advancements in diagnostic tools, the genomic landscape of hereditary hearing loss remains largely uncharacterized. One strategy to understand genome-wide aberrations includes the analysis of copy number variation that can be mapped using SNP-microarray technology. A growing collection of literature has begun to uncover the importance of copy number variation in hereditary hearing loss. more...

Organism:

Homo sapiens

Type:

Genome variation profiling by SNP array

Platform:

GPL24663

108 Samples

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