From b8db4b4c80a5bbee164d3283d0e78e9a023537e1 Mon Sep 17 00:00:00 2001 From: Michael Baudis Date: Thu, 12 Sep 2024 11:38:07 +0200 Subject: [PATCH] Update index.md Fixing map plot link --- docs/index.md | 2 +- 1 file changed, 1 insertion(+), 1 deletion(-) diff --git a/docs/index.md b/docs/index.md index 492ea74..fd1c089 100644 --- a/docs/index.md +++ b/docs/index.md @@ -7,7 +7,7 @@ authors: # ELIXIR Human Copy Number Variation community -Among the different types of inherited and acquired genomic variants, regional genomic copy number variations (CNV) contribute - if measured by affected genomic sequences - contribute by far the largest amount of genomic changes, contributing both to many syndromic diseases as well as the vast majority of human cancers. The [website](http://hcnv.github.io) of the _Human Copy Number Variation Community_ +Among the different types of inherited and acquired genomic variants, regional genomic copy number variations (CNV) contribute - if measured by affected genomic sequences - contribute by far the largest amount of genomic changes, contributing both to many syndromic diseases as well as the vast majority of human cancers. The [website](http://hcnv.github.io) of the _Human Copy Number Variation Community_ (hCNV) is a resource originated in ELIXIR's h-CNV Community Implementation Study (2019-2021) with the aim to provide a resource hub and knowledge exchange space for scientists and practitioners working with - or being interested in - genomic copy number variations in health and diseases. However, the scope of the community extends beyond CNVs and includes definition of and work with other types of genomic variations with a focus on structural variants.