Chromosomal-Abnormalities.md

@@ -136,7 +136,7 @@
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 <td>Velocardiofacial syndrome</td>
-<td>GRCh38 (chr21q11.2:150000-160000:del)</td>
+<td>GRCh38 21q11.2(chr21:150000-160000del)</td>
 <td>Structural Variant</td>
 <td>The specific microdeletion(s) genomic variants should be provided as SV. Vague "some microdeletions somewhere in a band of the q-arm" not supported. Deletion of whole 22q11.2 cytoband supported via equivalent genomic coordinates; best as a deletion SV than an x0 CNV</td>
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