# Infinium Assay CNV Analysis using GenomeStudio or BlueFuse Multi Software Support Webinar Video

Infinium Copy Number Variations (CNV) are genomic alterations that result in an abnormal number of copies of one or more genes and can contribute to diseases. This support webinar video covers the following topics: how Infinium genotyping data is converted to copy number analysis; a demonstration showing how GenomeStudio and the plugin software cnvPartition generate CNV detection analysis; and a demonstration of BlueFuse Multi for CNV detection, and the effects of mosaicism on the data.

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{% embed url="<https://www.youtube.com/watch?v=L_8eCfcT6_E&ab_channel=Illumina>" %}

Video length: 48:50 min

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| *For any feedback or questions regarding this article (Illumina Knowledge Article #8067), contact Illumina Technical Support* [*techsupport@illumina.com*](mailto:techsupport@illumina.com?subject=Question%2FFeedback%20Regarding%20Illumina%20Knowledge%20Article%20#000008067%20-%20Microarray%20\&body=Dear%20Illumina%20Technical%20Support,%0D%0A%0D%0A)*.* |


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