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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1069605copy number variation1nstd99human GRCh37 chr11: 71,952,299-71,952,800 , GRCh38.p12 chr11: 72,241,255-72,241,756 PHOX2A

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