content edits

README.md

@@ -1,9 +1,10 @@
 # [hCNV Reference Resources](https://cnvar.org/cnv-reference-resources/)
-##### Data & tools for hCNV analysis with a focus on the distributed normal
+
+**Data & tools for hCNV analysis with a focus on the distributed normal**
 
 The site was started as a project of the [ELIXIR hCNV Community](https://cnvar.org)
 at the [Biohackathon Europe 2023](https://biohackathon-europe.org):
 
-    [A "batteries-included" open reference resource for human genomic copy number variants (CNV)](https://github.com/elixir-europe/biohackathon-projects-2023/tree/main/1)
+**[A "batteries-included" open reference resource for human genomic copy number variants (CNV)](https://github.com/elixir-europe/biohackathon-projects-2023/tree/main/1)**
 
-This sitecan b efound at [cnvar.org/cnv-reference-resources/](https://cnvar.org/cnv-reference-resources/).
+This sitecan be found at [cnvar.org/cnv-reference-resources/](https://cnvar.org/cnv-reference-resources/).

docs/beacon-queries.md

@@ -1,3 +1,9 @@
 # Beacon CNV Queries
 
+! hint "Beacon Project Query Documentation"
+
+    The Beacon [project's documentation](http://docs.genomebeacons.org/variant-queries/#beacon-range-queries) includes examples for current queries enabling
+    discovery of CNVs (in resources supporting these formats).
+
+
 ==TBD==

docs/data-resources.md

@@ -2,4 +2,9 @@
 
 ## 1000 Genomes Dragen
 
+While primarily focused on somatic variants from cancer genomics the Progenetix
+resource also contains [CNV data from the 1000 Genomes Project](https://aws.amazon.com/blogs/industries/dragen-reanalysis-of-the-1000-genomes-dataset-now-available-on-the-registry-of-open-data/).
+
+* [1000 Genomes CNV](https://progenetix.org/progenetix-cohorts/oneKgenomes/) at Progenetix
+
 ==TBD==